Name: rs1206502227
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.

rs1206502227

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr2:162179813-162179826 (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)₆ / del(T)₅ / del(T)₄ / delT…
del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / ins(T)₃₈ / ins(T)₄₁
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₆=0.00000 (0/10958, ALFA)
del(T)₄=0.00000 (0/10958, ALFA)
delTTT=0.00000 (0/10958, ALFA) (+ 9 more)
delTT=0.00000 (0/10958, ALFA)
delT=0.00000 (0/10958, ALFA)
dupT=0.00000 (0/10958, ALFA)
dupTT=0.00000 (0/10958, ALFA)
dupTTT=0.00000 (0/10958, ALFA)
dup(T)₄=0.00000 (0/10958, ALFA)
dup(T)₅=0.00000 (0/10958, ALFA)
dup(T)₆=0.00000 (0/10958, ALFA)
dup(T)₇=0.00000 (0/10958, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FAP : 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	HWEP
Total	Global	10958	TTTTTTTTTTTTTT=1.00000	TTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7036	TTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2628	TTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	102	TTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African American	Sub	2526	TTTTTTTTTTTTTT=1.0000	TTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	106	TTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	82	TTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	24	TTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	140	TTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	526	TTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	92	TTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	430	TTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	10958	(T)₁₄=1.00000	del(T)₆=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000
Allele Frequency Aggregator	European	Sub	7036	(T)₁₄=1.0000	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)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	African	Sub	2628	(T)₁₄=1.0000	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)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	526	(T)₁₄=1.000	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)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	430	(T)₁₄=1.000	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)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	140	(T)₁₄=1.000	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)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Asian	Sub	106	(T)₁₄=1.000	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)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	South Asian	Sub	92	(T)₁₄=1.00	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)₅=0.00, dup(T)₆=0.00, dup(T)₇=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 2	NC_000002.12:g.162179821_162179826del
GRCh38.p14 chr 2	NC_000002.12:g.162179822_162179826del
GRCh38.p14 chr 2	NC_000002.12:g.162179823_162179826del
GRCh38.p14 chr 2	NC_000002.12:g.162179824_162179826del
GRCh38.p14 chr 2	NC_000002.12:g.162179825_162179826del
GRCh38.p14 chr 2	NC_000002.12:g.162179826del
GRCh38.p14 chr 2	NC_000002.12:g.162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179825_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179824_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179823_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179822_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179821_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179820_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179819_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179818_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179817_162179826dup
GRCh38.p14 chr 2	NC_000002.12:g.162179826_162179827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 2	NC_000002.12:g.162179826_162179827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.163036331_163036336del
GRCh37.p13 chr 2	NC_000002.11:g.163036332_163036336del
GRCh37.p13 chr 2	NC_000002.11:g.163036333_163036336del
GRCh37.p13 chr 2	NC_000002.11:g.163036334_163036336del
GRCh37.p13 chr 2	NC_000002.11:g.163036335_163036336del
GRCh37.p13 chr 2	NC_000002.11:g.163036336del
GRCh37.p13 chr 2	NC_000002.11:g.163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036335_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036334_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036333_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036332_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036331_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036330_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036329_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036328_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036327_163036336dup
GRCh37.p13 chr 2	NC_000002.11:g.163036336_163036337insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.163036336_163036337insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
FAP RefSeqGene	NG_027991.1:g.68718_68723del
FAP RefSeqGene	NG_027991.1:g.68719_68723del
FAP RefSeqGene	NG_027991.1:g.68720_68723del
FAP RefSeqGene	NG_027991.1:g.68721_68723del
FAP RefSeqGene	NG_027991.1:g.68722_68723del
FAP RefSeqGene	NG_027991.1:g.68723del
FAP RefSeqGene	NG_027991.1:g.68723dup
FAP RefSeqGene	NG_027991.1:g.68722_68723dup
FAP RefSeqGene	NG_027991.1:g.68721_68723dup
FAP RefSeqGene	NG_027991.1:g.68720_68723dup
FAP RefSeqGene	NG_027991.1:g.68719_68723dup
FAP RefSeqGene	NG_027991.1:g.68718_68723dup
FAP RefSeqGene	NG_027991.1:g.68717_68723dup
FAP RefSeqGene	NG_027991.1:g.68716_68723dup
FAP RefSeqGene	NG_027991.1:g.68715_68723dup
FAP RefSeqGene	NG_027991.1:g.68714_68723dup
FAP RefSeqGene	NG_027991.1:g.68723_68724insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
FAP RefSeqGene	NG_027991.1:g.68723_68724insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: FAP, fibroblast activation protein alpha (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FAP transcript variant 2	NM_001291807.3:c.1794+359… NM_001291807.3:c.1794+3596_1794+3601del	N/A	Intron Variant
FAP transcript variant 1	NM_004460.5:c.1869+3596_1… NM_004460.5:c.1869+3596_1869+3601del	N/A	Intron Variant
FAP transcript variant X1	XM_011510796.4:c.1839+359… XM_011510796.4:c.1839+3596_1839+3601del	N/A	Intron Variant
FAP transcript variant X2	XM_011510797.4:c.	N/A	Genic Downstream Transcript Variant
FAP transcript variant X3	XM_017003585.3:c.	N/A	Genic Downstream Transcript Variant
FAP transcript variant X5	XR_001738668.3:n.	N/A	Genic Downstream Transcript Variant
FAP transcript variant X4	XR_922891.3: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)₁₄=	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	ins(T)₃₈	ins(T)₄₁
GRCh38.p14 chr 2	NC_000002.12:g.162179813_162179826=	NC_000002.12:g.162179821_162179826del	NC_000002.12:g.162179822_162179826del	NC_000002.12:g.162179823_162179826del	NC_000002.12:g.162179824_162179826del	NC_000002.12:g.162179825_162179826del	NC_000002.12:g.162179826del	NC_000002.12:g.162179826dup	NC_000002.12:g.162179825_162179826dup	NC_000002.12:g.162179824_162179826dup	NC_000002.12:g.162179823_162179826dup	NC_000002.12:g.162179822_162179826dup	NC_000002.12:g.162179821_162179826dup	NC_000002.12:g.162179820_162179826dup	NC_000002.12:g.162179819_162179826dup	NC_000002.12:g.162179818_162179826dup	NC_000002.12:g.162179817_162179826dup	NC_000002.12:g.162179826_162179827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:g.162179826_162179827insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 2	NC_000002.11:g.163036323_163036336=	NC_000002.11:g.163036331_163036336del	NC_000002.11:g.163036332_163036336del	NC_000002.11:g.163036333_163036336del	NC_000002.11:g.163036334_163036336del	NC_000002.11:g.163036335_163036336del	NC_000002.11:g.163036336del	NC_000002.11:g.163036336dup	NC_000002.11:g.163036335_163036336dup	NC_000002.11:g.163036334_163036336dup	NC_000002.11:g.163036333_163036336dup	NC_000002.11:g.163036332_163036336dup	NC_000002.11:g.163036331_163036336dup	NC_000002.11:g.163036330_163036336dup	NC_000002.11:g.163036329_163036336dup	NC_000002.11:g.163036328_163036336dup	NC_000002.11:g.163036327_163036336dup	NC_000002.11:g.163036336_163036337insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.11:g.163036336_163036337insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
FAP RefSeqGene	NG_027991.1:g.68710_68723=	NG_027991.1:g.68718_68723del	NG_027991.1:g.68719_68723del	NG_027991.1:g.68720_68723del	NG_027991.1:g.68721_68723del	NG_027991.1:g.68722_68723del	NG_027991.1:g.68723del	NG_027991.1:g.68723dup	NG_027991.1:g.68722_68723dup	NG_027991.1:g.68721_68723dup	NG_027991.1:g.68720_68723dup	NG_027991.1:g.68719_68723dup	NG_027991.1:g.68718_68723dup	NG_027991.1:g.68717_68723dup	NG_027991.1:g.68716_68723dup	NG_027991.1:g.68715_68723dup	NG_027991.1:g.68714_68723dup	NG_027991.1:g.68723_68724insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_027991.1:g.68723_68724insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
FAP transcript variant 2	NM_001291807.3:c.1794+3601=	NM_001291807.3:c.1794+3596_1794+3601del	NM_001291807.3:c.1794+3597_1794+3601del	NM_001291807.3:c.1794+3598_1794+3601del	NM_001291807.3:c.1794+3599_1794+3601del	NM_001291807.3:c.1794+3600_1794+3601del	NM_001291807.3:c.1794+3601del	NM_001291807.3:c.1794+3601dup	NM_001291807.3:c.1794+3600_1794+3601dup	NM_001291807.3:c.1794+3599_1794+3601dup	NM_001291807.3:c.1794+3598_1794+3601dup	NM_001291807.3:c.1794+3597_1794+3601dup	NM_001291807.3:c.1794+3596_1794+3601dup	NM_001291807.3:c.1794+3595_1794+3601dup	NM_001291807.3:c.1794+3594_1794+3601dup	NM_001291807.3:c.1794+3593_1794+3601dup	NM_001291807.3:c.1794+3592_1794+3601dup	NM_001291807.3:c.1794+3601_1794+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001291807.3:c.1794+3601_1794+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
FAP transcript	NM_004460.2:c.1869+3601=	NM_004460.2:c.1869+3596_1869+3601del	NM_004460.2:c.1869+3597_1869+3601del	NM_004460.2:c.1869+3598_1869+3601del	NM_004460.2:c.1869+3599_1869+3601del	NM_004460.2:c.1869+3600_1869+3601del	NM_004460.2:c.1869+3601del	NM_004460.2:c.1869+3601dup	NM_004460.2:c.1869+3600_1869+3601dup	NM_004460.2:c.1869+3599_1869+3601dup	NM_004460.2:c.1869+3598_1869+3601dup	NM_004460.2:c.1869+3597_1869+3601dup	NM_004460.2:c.1869+3596_1869+3601dup	NM_004460.2:c.1869+3595_1869+3601dup	NM_004460.2:c.1869+3594_1869+3601dup	NM_004460.2:c.1869+3593_1869+3601dup	NM_004460.2:c.1869+3592_1869+3601dup	NM_004460.2:c.1869+3601_1869+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_004460.2:c.1869+3601_1869+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
FAP transcript variant 1	NM_004460.5:c.1869+3601=	NM_004460.5:c.1869+3596_1869+3601del	NM_004460.5:c.1869+3597_1869+3601del	NM_004460.5:c.1869+3598_1869+3601del	NM_004460.5:c.1869+3599_1869+3601del	NM_004460.5:c.1869+3600_1869+3601del	NM_004460.5:c.1869+3601del	NM_004460.5:c.1869+3601dup	NM_004460.5:c.1869+3600_1869+3601dup	NM_004460.5:c.1869+3599_1869+3601dup	NM_004460.5:c.1869+3598_1869+3601dup	NM_004460.5:c.1869+3597_1869+3601dup	NM_004460.5:c.1869+3596_1869+3601dup	NM_004460.5:c.1869+3595_1869+3601dup	NM_004460.5:c.1869+3594_1869+3601dup	NM_004460.5:c.1869+3593_1869+3601dup	NM_004460.5:c.1869+3592_1869+3601dup	NM_004460.5:c.1869+3601_1869+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_004460.5:c.1869+3601_1869+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
FAP transcript variant X1	XM_005246378.1:c.1794+3601=	XM_005246378.1:c.1794+3596_1794+3601del	XM_005246378.1:c.1794+3597_1794+3601del	XM_005246378.1:c.1794+3598_1794+3601del	XM_005246378.1:c.1794+3599_1794+3601del	XM_005246378.1:c.1794+3600_1794+3601del	XM_005246378.1:c.1794+3601del	XM_005246378.1:c.1794+3601dup	XM_005246378.1:c.1794+3600_1794+3601dup	XM_005246378.1:c.1794+3599_1794+3601dup	XM_005246378.1:c.1794+3598_1794+3601dup	XM_005246378.1:c.1794+3597_1794+3601dup	XM_005246378.1:c.1794+3596_1794+3601dup	XM_005246378.1:c.1794+3595_1794+3601dup	XM_005246378.1:c.1794+3594_1794+3601dup	XM_005246378.1:c.1794+3593_1794+3601dup	XM_005246378.1:c.1794+3592_1794+3601dup	XM_005246378.1:c.1794+3601_1794+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005246378.1:c.1794+3601_1794+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
FAP transcript variant X1	XM_011510796.4:c.1839+3601=	XM_011510796.4:c.1839+3596_1839+3601del	XM_011510796.4:c.1839+3597_1839+3601del	XM_011510796.4:c.1839+3598_1839+3601del	XM_011510796.4:c.1839+3599_1839+3601del	XM_011510796.4:c.1839+3600_1839+3601del	XM_011510796.4:c.1839+3601del	XM_011510796.4:c.1839+3601dup	XM_011510796.4:c.1839+3600_1839+3601dup	XM_011510796.4:c.1839+3599_1839+3601dup	XM_011510796.4:c.1839+3598_1839+3601dup	XM_011510796.4:c.1839+3597_1839+3601dup	XM_011510796.4:c.1839+3596_1839+3601dup	XM_011510796.4:c.1839+3595_1839+3601dup	XM_011510796.4:c.1839+3594_1839+3601dup	XM_011510796.4:c.1839+3593_1839+3601dup	XM_011510796.4:c.1839+3592_1839+3601dup	XM_011510796.4:c.1839+3601_1839+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	XM_011510796.4:c.1839+3601_1839+3602insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

40 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss96731932	Oct 11, 2018 (152)
2	URBANLAB	ss3647192609	Oct 11, 2018 (152)
3	EVA_DECODE	ss3705299434	Jul 13, 2019 (153)
4	EVA_DECODE	ss3705299437	Jul 13, 2019 (153)
5	EVA_DECODE	ss3705299438	Jul 13, 2019 (153)
6	EVA_DECODE	ss3705299439	Jul 13, 2019 (153)
7	ACPOP	ss3729052086	Jul 13, 2019 (153)
8	ACPOP	ss3729052087	Jul 13, 2019 (153)
9	ACPOP	ss3729052088	Jul 13, 2019 (153)
10	KOGIC	ss3949377053	Apr 25, 2020 (154)
11	KOGIC	ss3949377054	Apr 25, 2020 (154)
12	GNOMAD	ss4054506827	Apr 26, 2021 (155)
13	GNOMAD	ss4054506837	Apr 26, 2021 (155)
14	GNOMAD	ss4054506838	Apr 26, 2021 (155)
15	GNOMAD	ss4054506839	Apr 26, 2021 (155)
16	GNOMAD	ss4054506840	Apr 26, 2021 (155)
17	GNOMAD	ss4054506841	Apr 26, 2021 (155)
18	GNOMAD	ss4054506842	Apr 26, 2021 (155)
19	GNOMAD	ss4054506843	Apr 26, 2021 (155)
20	GNOMAD	ss4054506844	Apr 26, 2021 (155)
21	GNOMAD	ss4054506845	Apr 26, 2021 (155)
22	GNOMAD	ss4054506846	Apr 26, 2021 (155)
23	GNOMAD	ss4054506847	Apr 26, 2021 (155)
24	GNOMAD	ss4054506848	Apr 26, 2021 (155)
25	GNOMAD	ss4054506849	Apr 26, 2021 (155)
26	GNOMAD	ss4054506850	Apr 26, 2021 (155)
27	GNOMAD	ss4054506851	Apr 26, 2021 (155)
28	GNOMAD	ss4054506852	Apr 26, 2021 (155)
29	GNOMAD	ss4054506853	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5154830115	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5154830116	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5154830117	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5154830118	Apr 26, 2021 (155)
34	HUGCELL_USP	ss5450486587	Oct 12, 2022 (156)
35	HUGCELL_USP	ss5450486590	Oct 12, 2022 (156)
36	HUGCELL_USP	ss5450486591	Oct 12, 2022 (156)
37	TOMMO_GENOMICS	ss5685232454	Oct 12, 2022 (156)
38	TOMMO_GENOMICS	ss5685232455	Oct 12, 2022 (156)
39	TOMMO_GENOMICS	ss5685232457	Oct 12, 2022 (156)
40	TOMMO_GENOMICS	ss5685232458	Oct 12, 2022 (156)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 80014378 (NC_000002.12:162179812::T 271/83884) Row 80014388 (NC_000002.12:162179812::TT 115/83896) Row 80014389 (NC_000002.12:162179812::TTT 238/83900)...	-	Apr 26, 2021 (155)
59	Korean Genome Project Submission ignored due to conflicting rows: Row 5755054 (NC_000002.12:162179814:T: 31/1798) Row 5755055 (NC_000002.12:162179813:TT: 22/1798)	-	Apr 25, 2020 (154)
60	Korean Genome Project Submission ignored due to conflicting rows: Row 5755054 (NC_000002.12:162179814:T: 31/1798) Row 5755055 (NC_000002.12:162179813:TT: 22/1798)	-	Apr 25, 2020 (154)
61	Northern Sweden Submission ignored due to conflicting rows: Row 2336951 (NC_000002.11:163036322::TTTT 9/560) Row 2336952 (NC_000002.11:163036322:TT: 9/560) Row 2336953 (NC_000002.11:163036322::TTT 2/560)	-	Jul 13, 2019 (153)
62	Northern Sweden Submission ignored due to conflicting rows: Row 2336951 (NC_000002.11:163036322::TTTT 9/560) Row 2336952 (NC_000002.11:163036322:TT: 9/560) Row 2336953 (NC_000002.11:163036322::TTT 2/560)	-	Jul 13, 2019 (153)
63	Northern Sweden Submission ignored due to conflicting rows: Row 2336951 (NC_000002.11:163036322::TTTT 9/560) Row 2336952 (NC_000002.11:163036322:TT: 9/560) Row 2336953 (NC_000002.11:163036322::TTT 2/560)	-	Jul 13, 2019 (153)
64	8.3KJPN Submission ignored due to conflicting rows: Row 12799422 (NC_000002.11:163036322:TT: 147/16728) Row 12799423 (NC_000002.11:163036322:T: 359/16728) Row 12799424 (NC_000002.11:163036322::TTTT 1/16728)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 12799422 (NC_000002.11:163036322:TT: 147/16728) Row 12799423 (NC_000002.11:163036322:T: 359/16728) Row 12799424 (NC_000002.11:163036322::TTTT 1/16728)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 12799422 (NC_000002.11:163036322:TT: 147/16728) Row 12799423 (NC_000002.11:163036322:T: 359/16728) Row 12799424 (NC_000002.11:163036322::TTTT 1/16728)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 12799422 (NC_000002.11:163036322:TT: 147/16728) Row 12799423 (NC_000002.11:163036322:T: 359/16728) Row 12799424 (NC_000002.11:163036322::TTTT 1/16728)...	-	Apr 26, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 19069558 (NC_000002.12:162179812:TT: 234/28222) Row 19069559 (NC_000002.12:162179812:T: 594/28222) Row 19069561 (NC_000002.12:162179812::T 12/28222)...	-	Oct 12, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 19069558 (NC_000002.12:162179812:TT: 234/28222) Row 19069559 (NC_000002.12:162179812:T: 594/28222) Row 19069561 (NC_000002.12:162179812::T 12/28222)...	-	Oct 12, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 19069558 (NC_000002.12:162179812:TT: 234/28222) Row 19069559 (NC_000002.12:162179812:T: 594/28222) Row 19069561 (NC_000002.12:162179812::T 12/28222)...	-	Oct 12, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 19069558 (NC_000002.12:162179812:TT: 234/28222) Row 19069559 (NC_000002.12:162179812:T: 594/28222) Row 19069561 (NC_000002.12:162179812::T 12/28222)...	-	Oct 12, 2022 (156)
72	ALFA	NC_000002.12 - 162179813	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
ss4054506853	NC_000002.12:162179812:TTTTTT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4054506852	NC_000002.12:162179812:TTTTT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss3705299434, ss4054506851	NC_000002.12:162179812:TTTT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss5154830118	NC_000002.11:163036322:TTT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4054506850	NC_000002.12:162179812:TTT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3729052087, ss5154830115	NC_000002.11:163036322:TT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4054506849, ss5450486590, ss5685232454	NC_000002.12:162179812:TT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3949377054	NC_000002.12:162179813:TT:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss5154830116	NC_000002.11:163036322:T:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4054506848, ss5450486587, ss5685232455	NC_000002.12:162179812:T:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3949377053	NC_000002.12:162179814:T:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3705299437	NC_000002.12:162179815:T:	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3647192609, ss4054506827, ss5685232457	NC_000002.12:162179812::T	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3705299438	NC_000002.12:162179816::T	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss96731932	NT_005403.17:13245740::T	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4054506837, ss5685232458	NC_000002.12:162179812::TT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3705299439	NC_000002.12:162179816::TT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3729052088	NC_000002.11:163036322::TTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4054506838	NC_000002.12:162179812::TTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3729052086, ss5154830117	NC_000002.11:163036322::TTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4054506839, ss5450486591	NC_000002.12:162179812::TTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4054506840	NC_000002.12:162179812::TTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4054506841	NC_000002.12:162179812::TTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4054506842	NC_000002.12:162179812::TTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10879192831	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4054506843	NC_000002.12:162179812::TTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4054506844	NC_000002.12:162179812::TTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4054506845	NC_000002.12:162179812::TTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4054506846	NC_000002.12:162179812::TTTTTTTTTT… NC_000002.12:162179812::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4054506847	NC_000002.12:162179812::TTTTTTTTTT… NC_000002.12:162179812::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000002.12:162179812:TTTTTTTTTTT… NC_000002.12:162179812:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs1206502227

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

rs1206502227