Name: rs34602155
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.

rs34602155

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:119656379-119656398 (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)₁₁ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₁ / del(T)₁₀ / del(T)₉ / del(T)₈ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.03681 (462/12552, ALFA)
(T)₂₀=0.50 (20/40, GENOME_DK)
dupT=0.50 (20/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BAG3 : 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	12552	TTTTTTTTTTTTTTTTTTTT=0.94447	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00016, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.01769, TTTTTTTTTTTTTTTTTTTTT=0.03681, TTTTTTTTTTTTTTTTTTTTTT=0.00064, TTTTTTTTTTTTTTTTTTTTTTTT=0.00024, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.941283	0.010586	0.048131	32
European	Sub	10028	TTTTTTTTTTTTTTTTTTTT=0.93069	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00020, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.02204, TTTTTTTTTTTTTTTTTTTTT=0.04597, TTTTTTTTTTTTTTTTTTTTTT=0.00080, TTTTTTTTTTTTTTTTTTTTTTTT=0.00030, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.926019	0.013375	0.060606	32
African	Sub	1628	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	62	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1566	TTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	44	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	38	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	6	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	96	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	366	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	56	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	334	TTTTTTTTTTTTTTTTTTTT=0.994	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTT=0.003, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.993976	0.0	0.006024	0

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12552	(T)₂₀=0.94447	del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, delTTT=0.00016, delTT=0.00000, delT=0.01769, dupT=0.03681, dupTT=0.00064, dupTTT=0.00000, dup(T)₄=0.00024, dup(T)₅=0.00000
Allele Frequency Aggregator	European	Sub	10028	(T)₂₀=0.93069	del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, delTTT=0.00020, delTT=0.00000, delT=0.02204, dupT=0.04597, dupTT=0.00080, dupTTT=0.00000, dup(T)₄=0.00030, dup(T)₅=0.00000
Allele Frequency Aggregator	African	Sub	1628	(T)₂₀=1.0000	del(T)₁₁=0.0000, del(T)₁₀=0.0000, del(T)₉=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
Allele Frequency Aggregator	Latin American 2	Sub	366	(T)₂₀=1.000	del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=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
Allele Frequency Aggregator	Other	Sub	334	(T)₂₀=0.994	del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, delTTT=0.000, delTT=0.000, delT=0.003, dupT=0.003, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	96	(T)₂₀=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=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
Allele Frequency Aggregator	South Asian	Sub	56	(T)₂₀=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=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
Allele Frequency Aggregator	Asian	Sub	44	(T)₂₀=1.00	del(T)₁₁=0.00, del(T)₁₀=0.00, del(T)₉=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
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.50

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 10	NC_000010.11:g.119656388_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656389_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656390_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656391_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656394_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656395_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656396_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656397_119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656398del
GRCh38.p14 chr 10	NC_000010.11:g.119656398dup
GRCh38.p14 chr 10	NC_000010.11:g.119656397_119656398dup
GRCh38.p14 chr 10	NC_000010.11:g.119656396_119656398dup
GRCh38.p14 chr 10	NC_000010.11:g.119656395_119656398dup
GRCh38.p14 chr 10	NC_000010.11:g.119656394_119656398dup
GRCh38.p14 chr 10	NC_000010.11:g.119656393_119656398dup
GRCh37.p13 chr 10	NC_000010.10:g.121415900_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415901_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415902_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415903_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415906_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415907_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415908_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415909_121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415910del
GRCh37.p13 chr 10	NC_000010.10:g.121415910dup
GRCh37.p13 chr 10	NC_000010.10:g.121415909_121415910dup
GRCh37.p13 chr 10	NC_000010.10:g.121415908_121415910dup
GRCh37.p13 chr 10	NC_000010.10:g.121415907_121415910dup
GRCh37.p13 chr 10	NC_000010.10:g.121415906_121415910dup
GRCh37.p13 chr 10	NC_000010.10:g.121415905_121415910dup
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10019_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10020_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10021_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10022_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10025_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10026_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10027_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10028_10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10029del
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10029dup
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10028_10029dup
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10027_10029dup
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10026_10029dup
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10025_10029dup
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10024_10029dup

Gene: BAG3, BAG cochaperone 3 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BAG3 transcript	NM_004281.4:c.180+4533_18… NM_004281.4:c.180+4533_180+4543del	N/A	Intron Variant
BAG3 transcript variant X1	XM_005270287.2:c.180+4533… XM_005270287.2:c.180+4533_180+4543del	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)₂₀=	del(T)₁₁	del(T)₁₀	del(T)₉	del(T)₈	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆
GRCh38.p14 chr 10	NC_000010.11:g.119656379_119656398=	NC_000010.11:g.119656388_119656398del	NC_000010.11:g.119656389_119656398del	NC_000010.11:g.119656390_119656398del	NC_000010.11:g.119656391_119656398del	NC_000010.11:g.119656394_119656398del	NC_000010.11:g.119656395_119656398del	NC_000010.11:g.119656396_119656398del	NC_000010.11:g.119656397_119656398del	NC_000010.11:g.119656398del	NC_000010.11:g.119656398dup	NC_000010.11:g.119656397_119656398dup	NC_000010.11:g.119656396_119656398dup	NC_000010.11:g.119656395_119656398dup	NC_000010.11:g.119656394_119656398dup	NC_000010.11:g.119656393_119656398dup
GRCh37.p13 chr 10	NC_000010.10:g.121415891_121415910=	NC_000010.10:g.121415900_121415910del	NC_000010.10:g.121415901_121415910del	NC_000010.10:g.121415902_121415910del	NC_000010.10:g.121415903_121415910del	NC_000010.10:g.121415906_121415910del	NC_000010.10:g.121415907_121415910del	NC_000010.10:g.121415908_121415910del	NC_000010.10:g.121415909_121415910del	NC_000010.10:g.121415910del	NC_000010.10:g.121415910dup	NC_000010.10:g.121415909_121415910dup	NC_000010.10:g.121415908_121415910dup	NC_000010.10:g.121415907_121415910dup	NC_000010.10:g.121415906_121415910dup	NC_000010.10:g.121415905_121415910dup
BAG3 RefSeqGene (LRG_742)	NG_016125.1:g.10010_10029=	NG_016125.1:g.10019_10029del	NG_016125.1:g.10020_10029del	NG_016125.1:g.10021_10029del	NG_016125.1:g.10022_10029del	NG_016125.1:g.10025_10029del	NG_016125.1:g.10026_10029del	NG_016125.1:g.10027_10029del	NG_016125.1:g.10028_10029del	NG_016125.1:g.10029del	NG_016125.1:g.10029dup	NG_016125.1:g.10028_10029dup	NG_016125.1:g.10027_10029dup	NG_016125.1:g.10026_10029dup	NG_016125.1:g.10025_10029dup	NG_016125.1:g.10024_10029dup
BAG3 transcript	NM_004281.3:c.180+4524=	NM_004281.3:c.180+4533_180+4543del	NM_004281.3:c.180+4534_180+4543del	NM_004281.3:c.180+4535_180+4543del	NM_004281.3:c.180+4536_180+4543del	NM_004281.3:c.180+4539_180+4543del	NM_004281.3:c.180+4540_180+4543del	NM_004281.3:c.180+4541_180+4543del	NM_004281.3:c.180+4542_180+4543del	NM_004281.3:c.180+4543del	NM_004281.3:c.180+4543dup	NM_004281.3:c.180+4542_180+4543dup	NM_004281.3:c.180+4541_180+4543dup	NM_004281.3:c.180+4540_180+4543dup	NM_004281.3:c.180+4539_180+4543dup	NM_004281.3:c.180+4538_180+4543dup
BAG3 transcript	NM_004281.4:c.180+4524=	NM_004281.4:c.180+4533_180+4543del	NM_004281.4:c.180+4534_180+4543del	NM_004281.4:c.180+4535_180+4543del	NM_004281.4:c.180+4536_180+4543del	NM_004281.4:c.180+4539_180+4543del	NM_004281.4:c.180+4540_180+4543del	NM_004281.4:c.180+4541_180+4543del	NM_004281.4:c.180+4542_180+4543del	NM_004281.4:c.180+4543del	NM_004281.4:c.180+4543dup	NM_004281.4:c.180+4542_180+4543dup	NM_004281.4:c.180+4541_180+4543dup	NM_004281.4:c.180+4540_180+4543dup	NM_004281.4:c.180+4539_180+4543dup	NM_004281.4:c.180+4538_180+4543dup
BAG3 transcript variant X1	XM_005270287.1:c.180+4524=	XM_005270287.1:c.180+4533_180+4543del	XM_005270287.1:c.180+4534_180+4543del	XM_005270287.1:c.180+4535_180+4543del	XM_005270287.1:c.180+4536_180+4543del	XM_005270287.1:c.180+4539_180+4543del	XM_005270287.1:c.180+4540_180+4543del	XM_005270287.1:c.180+4541_180+4543del	XM_005270287.1:c.180+4542_180+4543del	XM_005270287.1:c.180+4543del	XM_005270287.1:c.180+4543dup	XM_005270287.1:c.180+4542_180+4543dup	XM_005270287.1:c.180+4541_180+4543dup	XM_005270287.1:c.180+4540_180+4543dup	XM_005270287.1:c.180+4539_180+4543dup	XM_005270287.1:c.180+4538_180+4543dup
BAG3 transcript variant X1	XM_005270287.2:c.180+4524=	XM_005270287.2:c.180+4533_180+4543del	XM_005270287.2:c.180+4534_180+4543del	XM_005270287.2:c.180+4535_180+4543del	XM_005270287.2:c.180+4536_180+4543del	XM_005270287.2:c.180+4539_180+4543del	XM_005270287.2:c.180+4540_180+4543del	XM_005270287.2:c.180+4541_180+4543del	XM_005270287.2:c.180+4542_180+4543del	XM_005270287.2:c.180+4543del	XM_005270287.2:c.180+4543dup	XM_005270287.2:c.180+4542_180+4543dup	XM_005270287.2:c.180+4541_180+4543dup	XM_005270287.2:c.180+4540_180+4543dup	XM_005270287.2:c.180+4539_180+4543dup	XM_005270287.2:c.180+4538_180+4543dup

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#.

44 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39746522	Mar 15, 2006 (126)
2	ABI	ss39775069	Mar 14, 2006 (126)
3	HUMANGENOME_JCVI	ss95554767	Oct 12, 2018 (152)
4	HUMANGENOME_JCVI	ss95973930	Mar 15, 2016 (147)
5	HUMANGENOME_JCVI	ss97610095	Oct 12, 2018 (152)
6	PJP	ss294679836	May 09, 2011 (134)
7	EVA_GENOME_DK	ss1574268761	Apr 01, 2015 (144)
8	SWEGEN	ss3007251065	Nov 08, 2017 (151)
9	EVA	ss3832364364	Apr 26, 2020 (154)
10	GNOMAD	ss4226800235	Apr 26, 2021 (155)
11	GNOMAD	ss4226800236	Apr 26, 2021 (155)
12	GNOMAD	ss4226800237	Apr 26, 2021 (155)
13	GNOMAD	ss4226800238	Apr 26, 2021 (155)
14	GNOMAD	ss4226800239	Apr 26, 2021 (155)
15	GNOMAD	ss4226800240	Apr 26, 2021 (155)
16	GNOMAD	ss4226800242	Apr 26, 2021 (155)
17	GNOMAD	ss4226800243	Apr 26, 2021 (155)
18	GNOMAD	ss4226800244	Apr 26, 2021 (155)
19	GNOMAD	ss4226800245	Apr 26, 2021 (155)
20	GNOMAD	ss4226800246	Apr 26, 2021 (155)
21	GNOMAD	ss4226800247	Apr 26, 2021 (155)
22	GNOMAD	ss4226800248	Apr 26, 2021 (155)
23	GNOMAD	ss4226800249	Apr 26, 2021 (155)
24	TOPMED	ss4868735935	Apr 26, 2021 (155)
25	TOPMED	ss4868735936	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5199764962	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5199764963	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5199764964	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5199764965	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5199764966	Apr 26, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5285693086	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5285693087	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5285693089	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5481093556	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5481093557	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5481093558	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5481093559	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5481093560	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5746220141	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5746220142	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5746220144	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5746220145	Oct 16, 2022 (156)
43	TOMMO_GENOMICS	ss5746220146	Oct 16, 2022 (156)
44	EVA	ss5825046171	Oct 16, 2022 (156)
45	The Danish reference pan genome	NC_000010.10 - 121415891	Apr 26, 2020 (154)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 365840308 (NC_000010.11:119656378::T 14375/116946) Row 365840309 (NC_000010.11:119656378::TT 618/116938) Row 365840310 (NC_000010.11:119656378::TTT 17/116952)...	-	Apr 26, 2021 (155)
60	8.3KJPN Submission ignored due to conflicting rows: Row 57734269 (NC_000010.10:121415890::T 3536/16630) Row 57734270 (NC_000010.10:121415890:T: 507/16630) Row 57734271 (NC_000010.10:121415890::TT 36/16630)...	-	Apr 26, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 57734269 (NC_000010.10:121415890::T 3536/16630) Row 57734270 (NC_000010.10:121415890:T: 507/16630) Row 57734271 (NC_000010.10:121415890::TT 36/16630)...	-	Apr 26, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 57734269 (NC_000010.10:121415890::T 3536/16630) Row 57734270 (NC_000010.10:121415890:T: 507/16630) Row 57734271 (NC_000010.10:121415890::TT 36/16630)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 57734269 (NC_000010.10:121415890::T 3536/16630) Row 57734270 (NC_000010.10:121415890:T: 507/16630) Row 57734271 (NC_000010.10:121415890::TT 36/16630)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 57734269 (NC_000010.10:121415890::T 3536/16630) Row 57734270 (NC_000010.10:121415890:T: 507/16630) Row 57734271 (NC_000010.10:121415890::TT 36/16630)...	-	Apr 26, 2021 (155)
65	14KJPN Submission ignored due to conflicting rows: Row 80057245 (NC_000010.11:119656378::T 6729/28190) Row 80057246 (NC_000010.11:119656378:T: 1029/28190) Row 80057248 (NC_000010.11:119656378::TT 42/28190)...	-	Oct 16, 2022 (156)
66	14KJPN Submission ignored due to conflicting rows: Row 80057245 (NC_000010.11:119656378::T 6729/28190) Row 80057246 (NC_000010.11:119656378:T: 1029/28190) Row 80057248 (NC_000010.11:119656378::TT 42/28190)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 80057245 (NC_000010.11:119656378::T 6729/28190) Row 80057246 (NC_000010.11:119656378:T: 1029/28190) Row 80057248 (NC_000010.11:119656378::TT 42/28190)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 80057245 (NC_000010.11:119656378::T 6729/28190) Row 80057246 (NC_000010.11:119656378:T: 1029/28190) Row 80057248 (NC_000010.11:119656378::TT 42/28190)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 80057245 (NC_000010.11:119656378::T 6729/28190) Row 80057246 (NC_000010.11:119656378:T: 1029/28190) Row 80057248 (NC_000010.11:119656378::TT 42/28190)...	-	Oct 16, 2022 (156)
70	TopMed Submission ignored due to conflicting rows: Row 84281590 (NC_000010.11:119656378:TTTTTTTTT: 2/264690) Row 84281591 (NC_000010.11:119656378:TTTTTTTTTTT: 2/264690)	-	Apr 26, 2021 (155)
71	TopMed Submission ignored due to conflicting rows: Row 84281590 (NC_000010.11:119656378:TTTTTTTTT: 2/264690) Row 84281591 (NC_000010.11:119656378:TTTTTTTTTTT: 2/264690)	-	Apr 26, 2021 (155)
72	ALFA	NC_000010.11 - 119656379	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
ss4226800249, ss4868735936	NC_000010.11:119656378:TTTTTTTTTTT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4226800248, ss4868735935	NC_000010.11:119656378:TTTTTTTTT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4226800247	NC_000010.11:119656378:TTTTTTTT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4226800246	NC_000010.11:119656378:TTTTT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4226800245	NC_000010.11:119656378:TTTT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4226800244, ss5481093560	NC_000010.11:119656378:TTT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5199764966	NC_000010.10:121415890:TT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4226800243, ss5481093558, ss5746220146	NC_000010.11:119656378:TT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3007251065, ss3832364364, ss5199764963	NC_000010.10:121415890:T:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4226800242, ss5285693087, ss5481093556, ss5746220142	NC_000010.11:119656378:T:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss39746522	NT_030059.13:72220354:T:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss95973930	NT_030059.13:72220373:T:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294679836	NC_000010.9:121405881::T	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
268556, ss1574268761, ss5199764962	NC_000010.10:121415890::T	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4226800235, ss5285693086, ss5481093557, ss5746220141	NC_000010.11:119656378::T	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss39775069	NT_030059.13:72220354::T	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss97610095	NT_030059.13:72220373::T	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss95973930	NT_030059.13:72220373:T:TT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss95554767	NT_030059.13:72220374::T	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5199764964, ss5825046171	NC_000010.10:121415890::TT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4226800236, ss5285693089, ss5481093559, ss5746220144	NC_000010.11:119656378::TT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5199764965	NC_000010.10:121415890::TTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4226800237, ss5746220145	NC_000010.11:119656378::TTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4226800238	NC_000010.11:119656378::TTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4226800239	NC_000010.11:119656378::TTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
14325606472	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4226800240	NC_000010.11:119656378::TTTTTT	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3132097600	NC_000010.11:119656378:TTTTTTTTTT:	NC_000010.11:119656378:TTTTTTTTTTT… NC_000010.11:119656378:TTTTTTTTTTTTTTTTTTTT: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 rs34602155

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

rs34602155