Name: rs34069417
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.

rs34069417

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr1:84302338-84302355 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₈ / del(T)₇ / del(T)₆ / del(…
del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / insTTTAATCA(T)₂₆ / insTTTATGCA(T)₂₅ / ins(T)₄A(T)₂₉ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₁₄ / dup(T)₁₇ / ins(T)₂₈ / ins(T)₃₄
Variation Type: Indel Insertion and Deletion
Frequency: (T)₁₈=0.2532 (1268/5008, 1000G)
(T)₁₈=0.3953 (1802/4558, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SAMD13 : 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	4558	TTTTTTTTTTTTTTTTTT=0.3953	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.1145, TTTTTTTTTTTTTTTT=0.0059, TTTTTTTTTTTTTTTTT=0.4827, TTTTTTTTTTTTTTTTTTTTTTTT=0.0013, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTTTT=0.0000	0.388202	0.429775	0.182022	32
European	Sub	4424	TTTTTTTTTTTTTTTTTT=0.3779	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.1180, TTTTTTTTTTTTTTTT=0.0061, TTTTTTTTTTTTTTTTT=0.4964, TTTTTTTTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTTTT=0.0000	0.366025	0.446001	0.187974	32
African	Sub	96	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	94	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	2	TTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	14	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	0	TTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other	Sub	20	TTTTTTTTTTTTTTTTTT=0.80	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.20, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00	0.7	0.1	0.2	1

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
1000Genomes	Global	Study-wide	5008	(T)₁₈=0.2532	delT=0.7468
1000Genomes	African	Sub	1322	(T)₁₈=0.2988	delT=0.7012
1000Genomes	East Asian	Sub	1008	(T)₁₈=0.2470	delT=0.7530
1000Genomes	Europe	Sub	1006	(T)₁₈=0.2107	delT=0.7893
1000Genomes	South Asian	Sub	978	(T)₁₈=0.165	delT=0.835
1000Genomes	American	Sub	694	(T)₁₈=0.362	delT=0.638
Allele Frequency Aggregator	Total	Global	4558	(T)₁₈=0.3953	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.1145, delTT=0.0059, delT=0.4827, dupT=0.0000, dup(T)₆=0.0013, ins(T)₂₈=0.0002
Allele Frequency Aggregator	European	Sub	4424	(T)₁₈=0.3779	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.1180, delTT=0.0061, delT=0.4964, dupT=0.0000, dup(T)₆=0.0014, ins(T)₂₈=0.0002
Allele Frequency Aggregator	African	Sub	96	(T)₁₈=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₆=0.00, ins(T)₂₈=0.00
Allele Frequency Aggregator	Other	Sub	20	(T)₁₈=0.80	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.20, dupT=0.00, dup(T)₆=0.00, ins(T)₂₈=0.00
Allele Frequency Aggregator	Latin American 2	Sub	14	(T)₁₈=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dup(T)₆=0.00, ins(T)₂₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	2	(T)₁₈=1.0	del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₆=0.0, ins(T)₂₈=0.0
Allele Frequency Aggregator	Asian	Sub	2	(T)₁₈=1.0	del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dup(T)₆=0.0, ins(T)₂₈=0.0
Allele Frequency Aggregator	South Asian	Sub	0	(T)₁₈=0	del(T)₈=0, del(T)₇=0, del(T)₆=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dup(T)₆=0, ins(T)₂₈=0

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 1	NC_000001.11:g.84302348_84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302349_84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302350_84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302351_84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302352_84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302353_84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302354_84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302355del
GRCh38.p14 chr 1	NC_000001.11:g.84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302354_84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302353_84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302338_84302355T[21]AATCATTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 1	NC_000001.11:g.84302338_84302355T[21]ATGCATTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 1	NC_000001.11:g.84302338_84302355T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 1	NC_000001.11:g.84302351_84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302350_84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302349_84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302342_84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302339_84302355dup
GRCh38.p14 chr 1	NC_000001.11:g.84302355_84302356insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 1	NC_000001.11:g.84302355_84302356insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.84768031_84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768032_84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768033_84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768034_84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768035_84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768036_84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768037_84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768038del
GRCh37.p13 chr 1	NC_000001.10:g.84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768037_84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768036_84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768021_84768038T[21]AATCATTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1	NC_000001.10:g.84768021_84768038T[21]ATGCATTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1	NC_000001.10:g.84768021_84768038T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 1	NC_000001.10:g.84768034_84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768033_84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768032_84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768025_84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768022_84768038dup
GRCh37.p13 chr 1	NC_000001.10:g.84768038_84768039insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.84768038_84768039insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: SAMD13, sterile alpha motif domain containing 13 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SAMD13 transcript variant 1	NM_001010971.3:c.11-855_1… NM_001010971.3:c.11-855_11-848del	N/A	Intron Variant
SAMD13 transcript variant 2	NM_001134663.2:c.-33+547_… NM_001134663.2:c.-33+547_-33+554del	N/A	Intron Variant
SAMD13 transcript variant 3	NM_001134664.2:c.	N/A	Genic Upstream Transcript Variant
SAMD13 transcript variant X1	XM_017000377.3:c.29-855_2… XM_017000377.3:c.29-855_29-848del	N/A	Intron 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)₁₈=	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	insTTTAATCA(T)₂₆	insTTTATGCA(T)₂₅	ins(T)₄A(T)₂₉	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₁₄	dup(T)₁₇	ins(T)₂₈	ins(T)₃₄
GRCh38.p14 chr 1	NC_000001.11:g.84302338_84302355=	NC_000001.11:g.84302348_84302355del	NC_000001.11:g.84302349_84302355del	NC_000001.11:g.84302350_84302355del	NC_000001.11:g.84302351_84302355del	NC_000001.11:g.84302352_84302355del	NC_000001.11:g.84302353_84302355del	NC_000001.11:g.84302354_84302355del	NC_000001.11:g.84302355del	NC_000001.11:g.84302355dup	NC_000001.11:g.84302354_84302355dup	NC_000001.11:g.84302353_84302355dup	NC_000001.11:g.84302338_84302355T[21]AATCATTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000001.11:g.84302338_84302355T[21]ATGCATTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000001.11:g.84302338_84302355T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000001.11:g.84302351_84302355dup	NC_000001.11:g.84302350_84302355dup	NC_000001.11:g.84302349_84302355dup	NC_000001.11:g.84302342_84302355dup	NC_000001.11:g.84302339_84302355dup	NC_000001.11:g.84302355_84302356insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:g.84302355_84302356insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 1	NC_000001.10:g.84768021_84768038=	NC_000001.10:g.84768031_84768038del	NC_000001.10:g.84768032_84768038del	NC_000001.10:g.84768033_84768038del	NC_000001.10:g.84768034_84768038del	NC_000001.10:g.84768035_84768038del	NC_000001.10:g.84768036_84768038del	NC_000001.10:g.84768037_84768038del	NC_000001.10:g.84768038del	NC_000001.10:g.84768038dup	NC_000001.10:g.84768037_84768038dup	NC_000001.10:g.84768036_84768038dup	NC_000001.10:g.84768021_84768038T[21]AATCATTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000001.10:g.84768021_84768038T[21]ATGCATTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000001.10:g.84768021_84768038T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000001.10:g.84768034_84768038dup	NC_000001.10:g.84768033_84768038dup	NC_000001.10:g.84768032_84768038dup	NC_000001.10:g.84768025_84768038dup	NC_000001.10:g.84768022_84768038dup	NC_000001.10:g.84768038_84768039insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.10:g.84768038_84768039insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAMD13 transcript variant 1	NM_001010971.2:c.11-865=	NM_001010971.2:c.11-855_11-848del	NM_001010971.2:c.11-854_11-848del	NM_001010971.2:c.11-853_11-848del	NM_001010971.2:c.11-852_11-848del	NM_001010971.2:c.11-851_11-848del	NM_001010971.2:c.11-850_11-848del	NM_001010971.2:c.11-849_11-848del	NM_001010971.2:c.11-848del	NM_001010971.2:c.11-848dup	NM_001010971.2:c.11-849_11-848dup	NM_001010971.2:c.11-850_11-848dup	NM_001010971.2:c.11-848_11-847insTTTAATCATTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.2:c.11-848_11-847insTTTATGCATTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.2:c.11-848_11-847insTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.2:c.11-852_11-848dup	NM_001010971.2:c.11-853_11-848dup	NM_001010971.2:c.11-854_11-848dup	NM_001010971.2:c.11-861_11-848dup	NM_001010971.2:c.11-864_11-848dup	NM_001010971.2:c.11-848_11-847insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.2:c.11-848_11-847insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAMD13 transcript variant 1	NM_001010971.3:c.11-865=	NM_001010971.3:c.11-855_11-848del	NM_001010971.3:c.11-854_11-848del	NM_001010971.3:c.11-853_11-848del	NM_001010971.3:c.11-852_11-848del	NM_001010971.3:c.11-851_11-848del	NM_001010971.3:c.11-850_11-848del	NM_001010971.3:c.11-849_11-848del	NM_001010971.3:c.11-848del	NM_001010971.3:c.11-848dup	NM_001010971.3:c.11-849_11-848dup	NM_001010971.3:c.11-850_11-848dup	NM_001010971.3:c.11-848_11-847insTTTAATCATTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.3:c.11-848_11-847insTTTATGCATTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.3:c.11-848_11-847insTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.3:c.11-852_11-848dup	NM_001010971.3:c.11-853_11-848dup	NM_001010971.3:c.11-854_11-848dup	NM_001010971.3:c.11-861_11-848dup	NM_001010971.3:c.11-864_11-848dup	NM_001010971.3:c.11-848_11-847insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001010971.3:c.11-848_11-847insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAMD13 transcript variant 2	NM_001134663.1:c.-33+537=	NM_001134663.1:c.-33+547_-33+554del	NM_001134663.1:c.-33+548_-33+554del	NM_001134663.1:c.-33+549_-33+554del	NM_001134663.1:c.-33+550_-33+554del	NM_001134663.1:c.-33+551_-33+554del	NM_001134663.1:c.-33+552_-33+554del	NM_001134663.1:c.-33+553_-33+554del	NM_001134663.1:c.-33+554del	NM_001134663.1:c.-33+554dup	NM_001134663.1:c.-33+553_-33+554dup	NM_001134663.1:c.-33+552_-33+554dup	NM_001134663.1:c.-33+554_-33+555insTTTAATCATTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.1:c.-33+554_-33+555insTTTATGCATTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.1:c.-33+554_-33+555insTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.1:c.-33+550_-33+554dup	NM_001134663.1:c.-33+549_-33+554dup	NM_001134663.1:c.-33+548_-33+554dup	NM_001134663.1:c.-33+541_-33+554dup	NM_001134663.1:c.-33+538_-33+554dup	NM_001134663.1:c.-33+554_-33+555insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.1:c.-33+554_-33+555insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAMD13 transcript variant 2	NM_001134663.2:c.-33+537=	NM_001134663.2:c.-33+547_-33+554del	NM_001134663.2:c.-33+548_-33+554del	NM_001134663.2:c.-33+549_-33+554del	NM_001134663.2:c.-33+550_-33+554del	NM_001134663.2:c.-33+551_-33+554del	NM_001134663.2:c.-33+552_-33+554del	NM_001134663.2:c.-33+553_-33+554del	NM_001134663.2:c.-33+554del	NM_001134663.2:c.-33+554dup	NM_001134663.2:c.-33+553_-33+554dup	NM_001134663.2:c.-33+552_-33+554dup	NM_001134663.2:c.-33+554_-33+555insTTTAATCATTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.2:c.-33+554_-33+555insTTTATGCATTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.2:c.-33+554_-33+555insTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.2:c.-33+550_-33+554dup	NM_001134663.2:c.-33+549_-33+554dup	NM_001134663.2:c.-33+548_-33+554dup	NM_001134663.2:c.-33+541_-33+554dup	NM_001134663.2:c.-33+538_-33+554dup	NM_001134663.2:c.-33+554_-33+555insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001134663.2:c.-33+554_-33+555insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
SAMD13 transcript variant X1	XM_017000377.3:c.29-865=	XM_017000377.3:c.29-855_29-848del	XM_017000377.3:c.29-854_29-848del	XM_017000377.3:c.29-853_29-848del	XM_017000377.3:c.29-852_29-848del	XM_017000377.3:c.29-851_29-848del	XM_017000377.3:c.29-850_29-848del	XM_017000377.3:c.29-849_29-848del	XM_017000377.3:c.29-848del	XM_017000377.3:c.29-848dup	XM_017000377.3:c.29-849_29-848dup	XM_017000377.3:c.29-850_29-848dup	XM_017000377.3:c.29-848_29-847insTTTAATCATTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017000377.3:c.29-848_29-847insTTTATGCATTTTTTTTTTTTTTTTTTTTTTTTT	XM_017000377.3:c.29-848_29-847insTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017000377.3:c.29-852_29-848dup	XM_017000377.3:c.29-853_29-848dup	XM_017000377.3:c.29-854_29-848dup	XM_017000377.3:c.29-861_29-848dup	XM_017000377.3:c.29-864_29-848dup	XM_017000377.3:c.29-848_29-847insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_017000377.3:c.29-848_29-847insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

62 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41096818	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95235046	Feb 05, 2009 (130)
3	BUSHMAN	ss193112905	Jul 04, 2010 (132)
4	GMI	ss288005405	May 04, 2012 (137)
5	PJP	ss294589092	May 09, 2011 (134)
6	BILGI_BIOE	ss666099380	Apr 25, 2013 (138)
7	SSIP	ss947024490	Aug 21, 2014 (142)
8	1000GENOMES	ss1367758945	Aug 21, 2014 (142)
9	EVA_UK10K_TWINSUK	ss1700880817	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1700880822	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1709936031	Apr 01, 2015 (144)
12	EVA_UK10K_ALSPAC	ss1709936033	Apr 01, 2015 (144)
13	EVA_UK10K_TWINSUK	ss1709936036	Apr 01, 2015 (144)
14	EVA_UK10K_TWINSUK	ss1709936038	Apr 01, 2015 (144)
15	SWEGEN	ss2987139095	Nov 08, 2017 (151)
16	BIOINF_KMB_FNS_UNIBA	ss3645054712	Oct 11, 2018 (152)
17	URBANLAB	ss3646708036	Oct 11, 2018 (152)
18	EVA_DECODE	ss3687165680	Jul 12, 2019 (153)
19	EVA_DECODE	ss3687165681	Jul 12, 2019 (153)
20	EVA_DECODE	ss3687165682	Jul 12, 2019 (153)
21	EVA_DECODE	ss3687165683	Jul 12, 2019 (153)
22	EVA_DECODE	ss3687165684	Jul 12, 2019 (153)
23	PACBIO	ss3783466351	Jul 12, 2019 (153)
24	PACBIO	ss3789116182	Jul 12, 2019 (153)
25	PACBIO	ss3789116183	Jul 12, 2019 (153)
26	PACBIO	ss3789116184	Jul 12, 2019 (153)
27	PACBIO	ss3793988965	Jul 12, 2019 (153)
28	PACBIO	ss3793988966	Jul 12, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3799456188	Jul 12, 2019 (153)
30	EVA	ss3826275133	Apr 25, 2020 (154)
31	KOGIC	ss3944896461	Apr 25, 2020 (154)
32	KOGIC	ss3944896462	Apr 25, 2020 (154)
33	KOGIC	ss3944896463	Apr 25, 2020 (154)
34	GNOMAD	ss3997187957	Apr 25, 2021 (155)
35	GNOMAD	ss3997187958	Apr 25, 2021 (155)
36	GNOMAD	ss3997187959	Apr 25, 2021 (155)
37	GNOMAD	ss3997187960	Apr 25, 2021 (155)
38	GNOMAD	ss3997187961	Apr 25, 2021 (155)
39	GNOMAD	ss3997187962	Apr 25, 2021 (155)
40	GNOMAD	ss3997187963	Apr 25, 2021 (155)
41	GNOMAD	ss3997187964	Apr 25, 2021 (155)
42	GNOMAD	ss3997187965	Apr 25, 2021 (155)
43	GNOMAD	ss3997187966	Apr 25, 2021 (155)
44	GNOMAD	ss3997187967	Apr 25, 2021 (155)
45	GNOMAD	ss3997187968	Apr 25, 2021 (155)
46	GNOMAD	ss3997187969	Apr 25, 2021 (155)
47	GNOMAD	ss3997187970	Apr 25, 2021 (155)
48	GNOMAD	ss3997187971	Apr 25, 2021 (155)
49	GNOMAD	ss3997187972	Apr 25, 2021 (155)
50	TOMMO_GENOMICS	ss5144848323	Apr 25, 2021 (155)
51	TOMMO_GENOMICS	ss5144848324	Apr 25, 2021 (155)
52	TOMMO_GENOMICS	ss5144848325	Apr 25, 2021 (155)
53	1000G_HIGH_COVERAGE	ss5242968712	Oct 12, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5242968713	Oct 12, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5242968714	Oct 12, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5242968715	Oct 12, 2022 (156)
57	HUGCELL_USP	ss5443958473	Oct 12, 2022 (156)
58	HUGCELL_USP	ss5443958474	Oct 12, 2022 (156)
59	HUGCELL_USP	ss5443958475	Oct 12, 2022 (156)
60	TOMMO_GENOMICS	ss5669875241	Oct 12, 2022 (156)
61	TOMMO_GENOMICS	ss5669875242	Oct 12, 2022 (156)
62	TOMMO_GENOMICS	ss5669875243	Oct 12, 2022 (156)
63	1000Genomes	NC_000001.10 - 84768021	Oct 11, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1342069 (NC_000001.10:84768020:TTT: 697/3854) Row 1342071 (NC_000001.10:84768021:T: 497/3854)	-	Oct 11, 2018 (152)
65	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 1342069 (NC_000001.10:84768020:TTT: 697/3854) Row 1342071 (NC_000001.10:84768021:T: 497/3854)	-	Oct 11, 2018 (152)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 17286089 (NC_000001.11:84302337::T 181/112748) Row 17286090 (NC_000001.11:84302337::TT 2/112754) Row 17286091 (NC_000001.11:84302337::TTT 1/112754)...	-	Apr 25, 2021 (155)
83	Korean Genome Project Submission ignored due to conflicting rows: Row 1274462 (NC_000001.11:84302339:T: 1104/1832) Row 1274463 (NC_000001.11:84302338:TT: 147/1832) Row 1274464 (NC_000001.11:84302337:TTT: 6/1832)	-	Apr 25, 2020 (154)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 1274462 (NC_000001.11:84302339:T: 1104/1832) Row 1274463 (NC_000001.11:84302338:TT: 147/1832) Row 1274464 (NC_000001.11:84302337:TTT: 6/1832)	-	Apr 25, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 1274462 (NC_000001.11:84302339:T: 1104/1832) Row 1274463 (NC_000001.11:84302338:TT: 147/1832) Row 1274464 (NC_000001.11:84302337:TTT: 6/1832)	-	Apr 25, 2020 (154)
86	8.3KJPN Submission ignored due to conflicting rows: Row 2817630 (NC_000001.10:84768020:T: 12496/16706) Row 2817631 (NC_000001.10:84768020:TT: 257/16706) Row 2817632 (NC_000001.10:84768020::T 2/16706)	-	Apr 25, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 2817630 (NC_000001.10:84768020:T: 12496/16706) Row 2817631 (NC_000001.10:84768020:TT: 257/16706) Row 2817632 (NC_000001.10:84768020::T 2/16706)	-	Apr 25, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 2817630 (NC_000001.10:84768020:T: 12496/16706) Row 2817631 (NC_000001.10:84768020:TT: 257/16706) Row 2817632 (NC_000001.10:84768020::T 2/16706)	-	Apr 25, 2021 (155)
89	14KJPN Submission ignored due to conflicting rows: Row 3712345 (NC_000001.11:84302337:T: 21892/28246) Row 3712346 (NC_000001.11:84302337:TT: 414/28246) Row 3712347 (NC_000001.11:84302337::T 7/28246)	-	Oct 12, 2022 (156)
90	14KJPN Submission ignored due to conflicting rows: Row 3712345 (NC_000001.11:84302337:T: 21892/28246) Row 3712346 (NC_000001.11:84302337:TT: 414/28246) Row 3712347 (NC_000001.11:84302337::T 7/28246)	-	Oct 12, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 3712345 (NC_000001.11:84302337:T: 21892/28246) Row 3712346 (NC_000001.11:84302337:TT: 414/28246) Row 3712347 (NC_000001.11:84302337::T 7/28246)	-	Oct 12, 2022 (156)
92	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1342069 (NC_000001.10:84768020:TTT: 636/3708) Row 1342071 (NC_000001.10:84768021:T: 446/3708)	-	Oct 11, 2018 (152)
93	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1342069 (NC_000001.10:84768020:TTT: 636/3708) Row 1342070 (NC_000001.10:84768022:T: 2626/3708) Row 1342071 (NC_000001.10:84768021:TT: 446/3708)	-	Apr 25, 2020 (154)
94	UK 10K study - Twins Submission ignored due to conflicting rows: Row 1342069 (NC_000001.10:84768020:TTT: 636/3708) Row 1342071 (NC_000001.10:84768021:T: 446/3708)	-	Oct 11, 2018 (152)
95	ALFA	NC_000001.11 - 84302338	Apr 25, 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
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss3997187972	NC_000001.11:84302337:TTTTTT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss3997187971	NC_000001.11:84302337:TTTTT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3687165680, ss3997187970	NC_000001.11:84302337:TTTT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1700880817, ss1700880822, ss2987139095, ss3783466351, ss3789116182, ss3793988965	NC_000001.10:84768020:TTT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3944896463, ss3997187969, ss5242968712, ss5443958473	NC_000001.11:84302337:TTT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3687165681	NC_000001.11:84302338:TTT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3789116183, ss5144848324	NC_000001.10:84768020:TT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss1709936033, ss1709936038	NC_000001.10:84768021:TT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3997187968, ss5242968714, ss5443958475, ss5669875242	NC_000001.11:84302337:TT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3944896462	NC_000001.11:84302338:TT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3687165682	NC_000001.11:84302339:TT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss288005405, ss294589092	NC_000001.9:84540608:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
2448974, ss666099380, ss1367758945, ss3789116184, ss3793988966, ss3826275133, ss5144848323	NC_000001.10:84768020:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
	NC_000001.10:84768021:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss947024490, ss1709936031, ss1709936036	NC_000001.10:84768022:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3645054712, ss3646708036, ss3799456188, ss5242968713, ss5443958474, ss5669875241	NC_000001.11:84302337:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3944896461	NC_000001.11:84302339:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3687165683	NC_000001.11:84302340:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss41096818, ss95235046	NT_032977.9:54739955:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss193112905	NT_032977.10:83716349:T:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5144848325	NC_000001.10:84768020::T	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3997187957, ss5242968715, ss5669875243	NC_000001.11:84302337::T	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3997187958	NC_000001.11:84302337::TT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3997187959	NC_000001.11:84302337::TTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187964	NC_000001.11:84302337::TTTTTTTTTTT… NC_000001.11:84302337::TTTTTTTTTTTTTTTTTTTTTAATCATTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTAATCATTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187965	NC_000001.11:84302337::TTTTTTTTTTT… NC_000001.11:84302337::TTTTTTTTTTTTTTTTTTTTTATGCATTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTATGCATTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187966	NC_000001.11:84302337::TTTTTTTTTTT… NC_000001.11:84302337::TTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3687165684	NC_000001.11:84302341::TTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187960	NC_000001.11:84302337::TTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187961	NC_000001.11:84302337::TTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187962	NC_000001.11:84302337::TTTTTTTTTTT… NC_000001.11:84302337::TTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187963	NC_000001.11:84302337::TTTTTTTTTTT… NC_000001.11:84302337::TTTTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
11411216102	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3997187967	NC_000001.11:84302337::TTTTTTTTTTT… NC_000001.11:84302337::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3081946737	NC_000001.11:84302337:TTTTTTTT:	NC_000001.11:84302337:TTTTTTTTTTTT… NC_000001.11:84302337:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT

Publications tab displays PubMed articles citing the variation as a listing of PMID, Title, Author, Year, Journal, ordered by Year, descending.

No publications for rs34069417

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

rs34069417