Name: rs35903374
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.

rs35903374

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:77870248-77870261 (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: delTTT / delTT / delT / dupT / dup…
delTTT / delTT / delT / dupT / dupTT / dupTTT / ins(T)₁₅ / ins(T)₁₆(GTTTTTT)₂TTTAACATCTTTATTC(T)₂₂
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.04955 (572/11545, ALFA)
delT=0.171 (102/598, NorthernSweden)
delT=0.23 (9/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PHTF2 : 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	11545	TTTTTTTTTTTTTT=0.94968	TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.04955, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00017, TTTTTTTTTTTTTTT=0.00061, TTTTTTTTTTTTTTTT=0.00000	0.909439	0.008534	0.082027	32
European	Sub	9561	TTTTTTTTTTTTTT=0.9392	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0598, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTTT=0.0000	0.890526	0.010316	0.099158	N/A
African	Sub	1016	TTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	30	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	986	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	88	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	68	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	90	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	434	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	74	TTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	282	TTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	11545	(T)₁₄=0.94968	delTT=0.00000, delT=0.04955, dupT=0.00061, dupTT=0.00000, ins(T)₁₅=0.00017
Allele Frequency Aggregator	European	Sub	9561	(T)₁₄=0.9392	delTT=0.0000, delT=0.0598, dupT=0.0007, dupTT=0.0000, ins(T)₁₅=0.0002
Allele Frequency Aggregator	African	Sub	1016	(T)₁₄=1.0000	delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, ins(T)₁₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	434	(T)₁₄=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, ins(T)₁₅=0.000
Allele Frequency Aggregator	Other	Sub	282	(T)₁₄=1.000	delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, ins(T)₁₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	90	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₁₅=0.00
Allele Frequency Aggregator	Asian	Sub	88	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₁₅=0.00
Allele Frequency Aggregator	South Asian	Sub	74	(T)₁₄=1.00	delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, ins(T)₁₅=0.00
Northern Sweden	ACPOP	Study-wide	598	(T)₁₄=0.829	delT=0.171
The Danish reference pan genome	Danish	Study-wide	40	(T)₁₄=0.78	delT=0.23

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 7	NC_000007.14:g.77870259_77870261del
GRCh38.p14 chr 7	NC_000007.14:g.77870260_77870261del
GRCh38.p14 chr 7	NC_000007.14:g.77870261del
GRCh38.p14 chr 7	NC_000007.14:g.77870261dup
GRCh38.p14 chr 7	NC_000007.14:g.77870260_77870261dup
GRCh38.p14 chr 7	NC_000007.14:g.77870259_77870261dup
GRCh38.p14 chr 7	NC_000007.14:g.77870261_77870262insTTTTTTTTTTTTTTT
GRCh38.p14 chr 7	NC_000007.14:g.77870248_77870261T[30]GTTTTTT[2]TTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 7	NC_000007.13:g.77499576_77499578del
GRCh37.p13 chr 7	NC_000007.13:g.77499577_77499578del
GRCh37.p13 chr 7	NC_000007.13:g.77499578del
GRCh37.p13 chr 7	NC_000007.13:g.77499578dup
GRCh37.p13 chr 7	NC_000007.13:g.77499577_77499578dup
GRCh37.p13 chr 7	NC_000007.13:g.77499576_77499578dup
GRCh37.p13 chr 7	NC_000007.13:g.77499578_77499579insTTTTTTTTTTTTTTT
GRCh37.p13 chr 7	NC_000007.13:g.77499565_77499578T[30]GTTTTTT[2]TTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT[1]

Gene: PHTF2, putative homeodomain transcription factor 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PHTF2 transcript variant 1	NM_001127357.2:c.46-23349… NM_001127357.2:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 3	NM_001127358.2:c.46-23349… NM_001127358.2:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 4	NM_001127359.2:c.46-23349… NM_001127359.2:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 5	NM_001127360.2:c.46-23349… NM_001127360.2:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 6	NM_001366081.1:c.46-23349… NM_001366081.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 7	NM_001366082.2:c.46-23349… NM_001366082.2:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 8	NM_001366083.1:c.46-23349… NM_001366083.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 9	NM_001366084.1:c.46-23349… NM_001366084.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 10	NM_001366085.2:c.46-23349… NM_001366085.2:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 11	NM_001366086.1:c.46-23349… NM_001366086.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 12	NM_001366087.1:c.46-23349… NM_001366087.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 13	NM_001366088.2:c.46-23349… NM_001366088.2:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 14	NM_001366089.1:c.147+1542… NM_001366089.1:c.147+15425_147+15427del	N/A	Intron Variant
PHTF2 transcript variant 15	NM_001395270.1:c.46-23349… NM_001395270.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 16	NM_001395271.1:c.46-23349… NM_001395271.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 17	NM_001395272.1:c.46-23349… NM_001395272.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant 2	NM_020432.5:c.46-23349_46… NM_020432.5:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant X1	XM_005250509.5:c.46-23349… XM_005250509.5:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant X2	XM_011516422.4:c.46-23349… XM_011516422.4:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant X5	XM_011516423.4:c.46-23349… XM_011516423.4:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant X3	XM_047420638.1:c.46-23349… XM_047420638.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant X4	XM_047420639.1:c.46-23349… XM_047420639.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant X6	XM_047420640.1:c.46-23349… XM_047420640.1:c.46-23349_46-23347del	N/A	Intron Variant
PHTF2 transcript variant X7	XM_011516424.3:c.	N/A	Genic Upstream 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=	delTTT	delTT	delT	dupT	dupTT	dupTTT	ins(T)₁₅	ins(T)₁₆(GTTTTTT)₂TTTAACATCTTTATTC(T)₂₂
GRCh38.p14 chr 7	NC_000007.14:g.77870248_77870261=	NC_000007.14:g.77870259_77870261del	NC_000007.14:g.77870260_77870261del	NC_000007.14:g.77870261del	NC_000007.14:g.77870261dup	NC_000007.14:g.77870260_77870261dup	NC_000007.14:g.77870259_77870261dup	NC_000007.14:g.77870261_77870262insTTTTTTTTTTTTTTT	NC_000007.14:g.77870248_77870261T[30]GTTTTTT[2]TTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 7	NC_000007.13:g.77499565_77499578=	NC_000007.13:g.77499576_77499578del	NC_000007.13:g.77499577_77499578del	NC_000007.13:g.77499578del	NC_000007.13:g.77499578dup	NC_000007.13:g.77499577_77499578dup	NC_000007.13:g.77499576_77499578dup	NC_000007.13:g.77499578_77499579insTTTTTTTTTTTTTTT	NC_000007.13:g.77499565_77499578T[30]GTTTTTT[2]TTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT[1]
PHTF2 transcript variant 1	NM_001127357.1:c.46-23360=	NM_001127357.1:c.46-23349_46-23347del	NM_001127357.1:c.46-23348_46-23347del	NM_001127357.1:c.46-23347del	NM_001127357.1:c.46-23347dup	NM_001127357.1:c.46-23348_46-23347dup	NM_001127357.1:c.46-23349_46-23347dup	NM_001127357.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127357.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 1	NM_001127357.2:c.46-23360=	NM_001127357.2:c.46-23349_46-23347del	NM_001127357.2:c.46-23348_46-23347del	NM_001127357.2:c.46-23347del	NM_001127357.2:c.46-23347dup	NM_001127357.2:c.46-23348_46-23347dup	NM_001127357.2:c.46-23349_46-23347dup	NM_001127357.2:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127357.2:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 3	NM_001127358.1:c.46-23360=	NM_001127358.1:c.46-23349_46-23347del	NM_001127358.1:c.46-23348_46-23347del	NM_001127358.1:c.46-23347del	NM_001127358.1:c.46-23347dup	NM_001127358.1:c.46-23348_46-23347dup	NM_001127358.1:c.46-23349_46-23347dup	NM_001127358.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127358.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 3	NM_001127358.2:c.46-23360=	NM_001127358.2:c.46-23349_46-23347del	NM_001127358.2:c.46-23348_46-23347del	NM_001127358.2:c.46-23347del	NM_001127358.2:c.46-23347dup	NM_001127358.2:c.46-23348_46-23347dup	NM_001127358.2:c.46-23349_46-23347dup	NM_001127358.2:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127358.2:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 4	NM_001127359.1:c.46-23360=	NM_001127359.1:c.46-23349_46-23347del	NM_001127359.1:c.46-23348_46-23347del	NM_001127359.1:c.46-23347del	NM_001127359.1:c.46-23347dup	NM_001127359.1:c.46-23348_46-23347dup	NM_001127359.1:c.46-23349_46-23347dup	NM_001127359.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127359.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 4	NM_001127359.2:c.46-23360=	NM_001127359.2:c.46-23349_46-23347del	NM_001127359.2:c.46-23348_46-23347del	NM_001127359.2:c.46-23347del	NM_001127359.2:c.46-23347dup	NM_001127359.2:c.46-23348_46-23347dup	NM_001127359.2:c.46-23349_46-23347dup	NM_001127359.2:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127359.2:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 5	NM_001127360.1:c.46-23360=	NM_001127360.1:c.46-23349_46-23347del	NM_001127360.1:c.46-23348_46-23347del	NM_001127360.1:c.46-23347del	NM_001127360.1:c.46-23347dup	NM_001127360.1:c.46-23348_46-23347dup	NM_001127360.1:c.46-23349_46-23347dup	NM_001127360.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127360.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 5	NM_001127360.2:c.46-23360=	NM_001127360.2:c.46-23349_46-23347del	NM_001127360.2:c.46-23348_46-23347del	NM_001127360.2:c.46-23347del	NM_001127360.2:c.46-23347dup	NM_001127360.2:c.46-23348_46-23347dup	NM_001127360.2:c.46-23349_46-23347dup	NM_001127360.2:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001127360.2:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 6	NM_001366081.1:c.46-23360=	NM_001366081.1:c.46-23349_46-23347del	NM_001366081.1:c.46-23348_46-23347del	NM_001366081.1:c.46-23347del	NM_001366081.1:c.46-23347dup	NM_001366081.1:c.46-23348_46-23347dup	NM_001366081.1:c.46-23349_46-23347dup	NM_001366081.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366081.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 7	NM_001366082.2:c.46-23360=	NM_001366082.2:c.46-23349_46-23347del	NM_001366082.2:c.46-23348_46-23347del	NM_001366082.2:c.46-23347del	NM_001366082.2:c.46-23347dup	NM_001366082.2:c.46-23348_46-23347dup	NM_001366082.2:c.46-23349_46-23347dup	NM_001366082.2:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366082.2:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 8	NM_001366083.1:c.46-23360=	NM_001366083.1:c.46-23349_46-23347del	NM_001366083.1:c.46-23348_46-23347del	NM_001366083.1:c.46-23347del	NM_001366083.1:c.46-23347dup	NM_001366083.1:c.46-23348_46-23347dup	NM_001366083.1:c.46-23349_46-23347dup	NM_001366083.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366083.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 9	NM_001366084.1:c.46-23360=	NM_001366084.1:c.46-23349_46-23347del	NM_001366084.1:c.46-23348_46-23347del	NM_001366084.1:c.46-23347del	NM_001366084.1:c.46-23347dup	NM_001366084.1:c.46-23348_46-23347dup	NM_001366084.1:c.46-23349_46-23347dup	NM_001366084.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366084.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 10	NM_001366085.2:c.46-23360=	NM_001366085.2:c.46-23349_46-23347del	NM_001366085.2:c.46-23348_46-23347del	NM_001366085.2:c.46-23347del	NM_001366085.2:c.46-23347dup	NM_001366085.2:c.46-23348_46-23347dup	NM_001366085.2:c.46-23349_46-23347dup	NM_001366085.2:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366085.2:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 11	NM_001366086.1:c.46-23360=	NM_001366086.1:c.46-23349_46-23347del	NM_001366086.1:c.46-23348_46-23347del	NM_001366086.1:c.46-23347del	NM_001366086.1:c.46-23347dup	NM_001366086.1:c.46-23348_46-23347dup	NM_001366086.1:c.46-23349_46-23347dup	NM_001366086.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366086.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 12	NM_001366087.1:c.46-23360=	NM_001366087.1:c.46-23349_46-23347del	NM_001366087.1:c.46-23348_46-23347del	NM_001366087.1:c.46-23347del	NM_001366087.1:c.46-23347dup	NM_001366087.1:c.46-23348_46-23347dup	NM_001366087.1:c.46-23349_46-23347dup	NM_001366087.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366087.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 13	NM_001366088.2:c.46-23360=	NM_001366088.2:c.46-23349_46-23347del	NM_001366088.2:c.46-23348_46-23347del	NM_001366088.2:c.46-23347del	NM_001366088.2:c.46-23347dup	NM_001366088.2:c.46-23348_46-23347dup	NM_001366088.2:c.46-23349_46-23347dup	NM_001366088.2:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001366088.2:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 14	NM_001366089.1:c.147+15414=	NM_001366089.1:c.147+15425_147+15427del	NM_001366089.1:c.147+15426_147+15427del	NM_001366089.1:c.147+15427del	NM_001366089.1:c.147+15427dup	NM_001366089.1:c.147+15426_147+15427dup	NM_001366089.1:c.147+15425_147+15427dup	NM_001366089.1:c.147+15427_147+15428insTTTTTTTTTTTTTTT	NM_001366089.1:c.147+15427_147+15428insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 15	NM_001395270.1:c.46-23360=	NM_001395270.1:c.46-23349_46-23347del	NM_001395270.1:c.46-23348_46-23347del	NM_001395270.1:c.46-23347del	NM_001395270.1:c.46-23347dup	NM_001395270.1:c.46-23348_46-23347dup	NM_001395270.1:c.46-23349_46-23347dup	NM_001395270.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001395270.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 16	NM_001395271.1:c.46-23360=	NM_001395271.1:c.46-23349_46-23347del	NM_001395271.1:c.46-23348_46-23347del	NM_001395271.1:c.46-23347del	NM_001395271.1:c.46-23347dup	NM_001395271.1:c.46-23348_46-23347dup	NM_001395271.1:c.46-23349_46-23347dup	NM_001395271.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001395271.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 17	NM_001395272.1:c.46-23360=	NM_001395272.1:c.46-23349_46-23347del	NM_001395272.1:c.46-23348_46-23347del	NM_001395272.1:c.46-23347del	NM_001395272.1:c.46-23347dup	NM_001395272.1:c.46-23348_46-23347dup	NM_001395272.1:c.46-23349_46-23347dup	NM_001395272.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_001395272.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 2	NM_020432.4:c.46-23360=	NM_020432.4:c.46-23349_46-23347del	NM_020432.4:c.46-23348_46-23347del	NM_020432.4:c.46-23347del	NM_020432.4:c.46-23347dup	NM_020432.4:c.46-23348_46-23347dup	NM_020432.4:c.46-23349_46-23347dup	NM_020432.4:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_020432.4:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant 2	NM_020432.5:c.46-23360=	NM_020432.5:c.46-23349_46-23347del	NM_020432.5:c.46-23348_46-23347del	NM_020432.5:c.46-23347del	NM_020432.5:c.46-23347dup	NM_020432.5:c.46-23348_46-23347dup	NM_020432.5:c.46-23349_46-23347dup	NM_020432.5:c.46-23347_46-23346insTTTTTTTTTTTTTTT	NM_020432.5:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X1	XM_005250508.1:c.46-23360=	XM_005250508.1:c.46-23349_46-23347del	XM_005250508.1:c.46-23348_46-23347del	XM_005250508.1:c.46-23347del	XM_005250508.1:c.46-23347dup	XM_005250508.1:c.46-23348_46-23347dup	XM_005250508.1:c.46-23349_46-23347dup	XM_005250508.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_005250508.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X2	XM_005250509.1:c.46-23360=	XM_005250509.1:c.46-23349_46-23347del	XM_005250509.1:c.46-23348_46-23347del	XM_005250509.1:c.46-23347del	XM_005250509.1:c.46-23347dup	XM_005250509.1:c.46-23348_46-23347dup	XM_005250509.1:c.46-23349_46-23347dup	XM_005250509.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_005250509.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X1	XM_005250509.5:c.46-23360=	XM_005250509.5:c.46-23349_46-23347del	XM_005250509.5:c.46-23348_46-23347del	XM_005250509.5:c.46-23347del	XM_005250509.5:c.46-23347dup	XM_005250509.5:c.46-23348_46-23347dup	XM_005250509.5:c.46-23349_46-23347dup	XM_005250509.5:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_005250509.5:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X2	XM_011516422.4:c.46-23360=	XM_011516422.4:c.46-23349_46-23347del	XM_011516422.4:c.46-23348_46-23347del	XM_011516422.4:c.46-23347del	XM_011516422.4:c.46-23347dup	XM_011516422.4:c.46-23348_46-23347dup	XM_011516422.4:c.46-23349_46-23347dup	XM_011516422.4:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_011516422.4:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X5	XM_011516423.4:c.46-23360=	XM_011516423.4:c.46-23349_46-23347del	XM_011516423.4:c.46-23348_46-23347del	XM_011516423.4:c.46-23347del	XM_011516423.4:c.46-23347dup	XM_011516423.4:c.46-23348_46-23347dup	XM_011516423.4:c.46-23349_46-23347dup	XM_011516423.4:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_011516423.4:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X3	XM_047420638.1:c.46-23360=	XM_047420638.1:c.46-23349_46-23347del	XM_047420638.1:c.46-23348_46-23347del	XM_047420638.1:c.46-23347del	XM_047420638.1:c.46-23347dup	XM_047420638.1:c.46-23348_46-23347dup	XM_047420638.1:c.46-23349_46-23347dup	XM_047420638.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_047420638.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X4	XM_047420639.1:c.46-23360=	XM_047420639.1:c.46-23349_46-23347del	XM_047420639.1:c.46-23348_46-23347del	XM_047420639.1:c.46-23347del	XM_047420639.1:c.46-23347dup	XM_047420639.1:c.46-23348_46-23347dup	XM_047420639.1:c.46-23349_46-23347dup	XM_047420639.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_047420639.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT
PHTF2 transcript variant X6	XM_047420640.1:c.46-23360=	XM_047420640.1:c.46-23349_46-23347del	XM_047420640.1:c.46-23348_46-23347del	XM_047420640.1:c.46-23347del	XM_047420640.1:c.46-23347dup	XM_047420640.1:c.46-23348_46-23347dup	XM_047420640.1:c.46-23349_46-23347dup	XM_047420640.1:c.46-23347_46-23346insTTTTTTTTTTTTTTT	XM_047420640.1:c.46-23347_46-23346insTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT

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#.

31 SubSNP, 16 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42988378	Dec 03, 2013 (138)
2	HUMANGENOME_JCVI	ss95465574	Dec 05, 2013 (138)
3	PJP	ss295342547	May 09, 2011 (137)
4	SSMP	ss663800017	Apr 01, 2015 (144)
5	BILGI_BIOE	ss666404455	Apr 25, 2013 (138)
6	EVA_GENOME_DK	ss1577024032	Apr 01, 2015 (144)
7	HAMMER_LAB	ss1805068769	Sep 08, 2015 (146)
8	MCHAISSO	ss3066152281	Nov 08, 2017 (151)
9	EVA_DECODE	ss3720014428	Jul 13, 2019 (153)
10	EVA_DECODE	ss3720014429	Jul 13, 2019 (153)
11	EVA_DECODE	ss3720014430	Jul 13, 2019 (153)
12	ACPOP	ss3734774301	Jul 13, 2019 (153)
13	EVA	ss3830650735	Apr 26, 2020 (154)
14	GNOMAD	ss4166700233	Apr 26, 2021 (155)
15	GNOMAD	ss4166700234	Apr 26, 2021 (155)
16	GNOMAD	ss4166700235	Apr 26, 2021 (155)
17	GNOMAD	ss4166700236	Apr 26, 2021 (155)
18	GNOMAD	ss4166700237	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5183981640	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5183981641	Apr 26, 2021 (155)
21	TOMMO_GENOMICS	ss5183981642	Apr 26, 2021 (155)
22	1000G_HIGH_COVERAGE	ss5273509074	Oct 17, 2022 (156)
23	1000G_HIGH_COVERAGE	ss5273509076	Oct 17, 2022 (156)
24	1000G_HIGH_COVERAGE	ss5273509077	Oct 17, 2022 (156)
25	HUGCELL_USP	ss5470528794	Oct 17, 2022 (156)
26	HUGCELL_USP	ss5470528795	Oct 17, 2022 (156)
27	HUGCELL_USP	ss5470528796	Oct 17, 2022 (156)
28	TOMMO_GENOMICS	ss5724493527	Oct 17, 2022 (156)
29	TOMMO_GENOMICS	ss5724493528	Oct 17, 2022 (156)
30	TOMMO_GENOMICS	ss5724493529	Oct 17, 2022 (156)
31	EVA	ss5855960531	Oct 17, 2022 (156)
32	The Danish reference pan genome	NC_000007.13 - 77499565	Apr 26, 2020 (154)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 266202916 (NC_000007.14:77870247::T 1357/121692) Row 266202917 (NC_000007.14:77870247::TT 37/121754) Row 266202918 (NC_000007.14:77870247::TTT 1/121762)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 266202916 (NC_000007.14:77870247::T 1357/121692) Row 266202917 (NC_000007.14:77870247::TT 37/121754) Row 266202918 (NC_000007.14:77870247::TTT 1/121762)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 266202916 (NC_000007.14:77870247::T 1357/121692) Row 266202917 (NC_000007.14:77870247::TT 37/121754) Row 266202918 (NC_000007.14:77870247::TTT 1/121762)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 266202916 (NC_000007.14:77870247::T 1357/121692) Row 266202917 (NC_000007.14:77870247::TT 37/121754) Row 266202918 (NC_000007.14:77870247::TTT 1/121762)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 266202916 (NC_000007.14:77870247::T 1357/121692) Row 266202917 (NC_000007.14:77870247::TT 37/121754) Row 266202918 (NC_000007.14:77870247::TTT 1/121762)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 266202916 (NC_000007.14:77870247::T 1357/121692) Row 266202917 (NC_000007.14:77870247::TT 37/121754) Row 266202918 (NC_000007.14:77870247::TTT 1/121762)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 266202916 (NC_000007.14:77870247::T 1357/121692) Row 266202917 (NC_000007.14:77870247::TT 37/121754) Row 266202918 (NC_000007.14:77870247::TTT 1/121762)...	-	Apr 26, 2021 (155)
40	Northern Sweden	NC_000007.13 - 77499565	Jul 13, 2019 (153)
41	8.3KJPN Submission ignored due to conflicting rows: Row 41950947 (NC_000007.13:77499564:T: 444/16758) Row 41950948 (NC_000007.13:77499564::T 51/16758) Row 41950949 (NC_000007.13:77499564:TTT: 1/16758)	-	Apr 26, 2021 (155)
42	8.3KJPN Submission ignored due to conflicting rows: Row 41950947 (NC_000007.13:77499564:T: 444/16758) Row 41950948 (NC_000007.13:77499564::T 51/16758) Row 41950949 (NC_000007.13:77499564:TTT: 1/16758)	-	Apr 26, 2021 (155)
43	8.3KJPN Submission ignored due to conflicting rows: Row 41950947 (NC_000007.13:77499564:T: 444/16758) Row 41950948 (NC_000007.13:77499564::T 51/16758) Row 41950949 (NC_000007.13:77499564:TTT: 1/16758)	-	Apr 26, 2021 (155)
44	14KJPN Submission ignored due to conflicting rows: Row 58330631 (NC_000007.14:77870247:T: 764/28258) Row 58330632 (NC_000007.14:77870247::T 91/28258) Row 58330633 (NC_000007.14:77870247:TTT: 1/28258)	-	Oct 17, 2022 (156)
45	14KJPN Submission ignored due to conflicting rows: Row 58330631 (NC_000007.14:77870247:T: 764/28258) Row 58330632 (NC_000007.14:77870247::T 91/28258) Row 58330633 (NC_000007.14:77870247:TTT: 1/28258)	-	Oct 17, 2022 (156)
46	14KJPN Submission ignored due to conflicting rows: Row 58330631 (NC_000007.14:77870247:T: 764/28258) Row 58330632 (NC_000007.14:77870247::T 91/28258) Row 58330633 (NC_000007.14:77870247:TTT: 1/28258)	-	Oct 17, 2022 (156)
47	ALFA	NC_000007.14 - 77870248	Apr 26, 2021 (155)

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

Associated ID	History Updated (Build)
rs147525328	May 11, 2012 (137)
rs373963635	May 13, 2013 (138)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5183981642	NC_000007.13:77499564:TTT:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4166700237, ss5724493529	NC_000007.14:77870247:TTT:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3720014428, ss4166700236, ss5273509077, ss5470528796	NC_000007.14:77870247:TT:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
6283713672	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss295342547	NC_000007.12:77337500:T:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
1161580, 8059166, ss663800017, ss666404455, ss1577024032, ss1805068769, ss3734774301, ss3830650735, ss5183981640	NC_000007.13:77499564:T:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3066152281, ss5273509074, ss5470528795, ss5724493527, ss5855960531	NC_000007.14:77870247:T:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6283713672	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3720014429	NC_000007.14:77870248:T:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss42988378, ss95465574	NT_007933.15:15532420:T:	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5183981641	NC_000007.13:77499564::T	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4166700233, ss5273509076, ss5470528794, ss5724493528	NC_000007.14:77870247::T	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6283713672	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3720014430	NC_000007.14:77870249::T	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4166700234	NC_000007.14:77870247::TT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6283713672	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4166700235	NC_000007.14:77870247::TTT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6283713672	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000007.14:77870247::TTTTTTTTTTT… NC_000007.14:77870247::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTT	NC_000007.14:77870247:TTTTTTTTTTTT… NC_000007.14:77870247:TTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTGTTTTTTTTTAACATCTTTATTCTTTTTTTTTTTTTTTTTTTTTT	(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 rs35903374

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

rs35903374