Name: rs34202425
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.

rs34202425

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr21:14375492-14375513 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₂ / del(T)₈ / del(T)₆ / del…
del(T)₁₂ / del(T)₈ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₉ / dup(T)₁₁
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.1542 (954/6188, ALFA)
(T)₂₂=0.4740 (2374/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: HSPA13 : 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	6188	TTTTTTTTTTTTTTTTTTTTTT=0.5884	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0170, TTTTTTTTTTTTTTTTTTTT=0.1542, TTTTTTTTTTTTTTTTTTTTT=0.1065, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0086, TTTTTTTTTTTTTTTTTTTTTTTTT=0.1244, TTTTTTTTTTTTTTTTTTTTTTT=0.0010, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.735342	0.062937	0.201721	32
European	Sub	5220	TTTTTTTTTTTTTTTTTTTTTT=0.5130	TTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0199, TTTTTTTTTTTTTTTTTTTT=0.1824, TTTTTTTTTTTTTTTTTTTTT=0.1262, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0102, TTTTTTTTTTTTTTTTTTTTTTTTT=0.1471, TTTTTTTTTTTTTTTTTTTTTTT=0.0011, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.643687	0.08418	0.272134	32
African	Sub	718	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	38	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	680	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	20	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	136	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	70	TTTTTTTTTTTTTTTTTTTTTT=0.93	TTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.96875	0.03125	0.0	17

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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	6188	(T)₂₂=0.5884	del(T)₁₂=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0170, delTT=0.1542, delT=0.1065, dupT=0.0010, dupTT=0.0000, dupTTT=0.1244, dup(T)₄=0.0086, dup(T)₅=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	European	Sub	5220	(T)₂₂=0.5130	del(T)₁₂=0.0000, del(T)₈=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0199, delTT=0.1824, delT=0.1262, dupT=0.0011, dupTT=0.0000, dupTTT=0.1471, dup(T)₄=0.0102, dup(T)₅=0.0000, dup(T)₆=0.0000
Allele Frequency Aggregator	African	Sub	718	(T)₂₂=1.000	del(T)₁₂=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Latin American 2	Sub	136	(T)₂₂=1.000	del(T)₁₂=0.000, del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000
Allele Frequency Aggregator	Other	Sub	70	(T)₂₂=0.93	del(T)₁₂=0.00, del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.01, delTT=0.03, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.03, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(T)₂₂=1.00	del(T)₁₂=0.00, del(T)₈=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, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	Asian	Sub	14	(T)₂₂=1.00	del(T)₁₂=0.00, del(T)₈=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, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00
Allele Frequency Aggregator	South Asian	Sub	10	(T)₂₂=1.0	del(T)₁₂=0.0, del(T)₈=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, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0
1000Genomes	Global	Study-wide	5008	(T)₂₂=0.4740	delTT=0.5260
1000Genomes	African	Sub	1322	(T)₂₂=0.5976	delTT=0.4024
1000Genomes	East Asian	Sub	1008	(T)₂₂=0.4782	delTT=0.5218
1000Genomes	Europe	Sub	1006	(T)₂₂=0.3390	delTT=0.6610
1000Genomes	South Asian	Sub	978	(T)₂₂=0.416	delTT=0.584
1000Genomes	American	Sub	694	(T)₂₂=0.510	delTT=0.490

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 21	NC_000021.9:g.14375502_14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375506_14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375508_14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375509_14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375510_14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375511_14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375512_14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375513del
GRCh38.p14 chr 21	NC_000021.9:g.14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375512_14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375511_14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375510_14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375509_14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375508_14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375507_14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375505_14375513dup
GRCh38.p14 chr 21	NC_000021.9:g.14375503_14375513dup
GRCh37.p13 chr 21	NC_000021.8:g.15747823_15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747827_15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747829_15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747830_15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747831_15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747832_15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747833_15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747834del
GRCh37.p13 chr 21	NC_000021.8:g.15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747833_15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747832_15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747831_15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747830_15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747829_15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747828_15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747826_15747834dup
GRCh37.p13 chr 21	NC_000021.8:g.15747824_15747834dup

Gene: HSPA13, heat shock protein family A (Hsp70) member 13 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
HSPA13 transcript	NM_006948.5:c.748+149_748… NM_006948.5:c.748+149_748+160del	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)₂₂=	del(T)₁₂	del(T)₈	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₉	dup(T)₁₁
GRCh38.p14 chr 21	NC_000021.9:g.14375492_14375513=	NC_000021.9:g.14375502_14375513del	NC_000021.9:g.14375506_14375513del	NC_000021.9:g.14375508_14375513del	NC_000021.9:g.14375509_14375513del	NC_000021.9:g.14375510_14375513del	NC_000021.9:g.14375511_14375513del	NC_000021.9:g.14375512_14375513del	NC_000021.9:g.14375513del	NC_000021.9:g.14375513dup	NC_000021.9:g.14375512_14375513dup	NC_000021.9:g.14375511_14375513dup	NC_000021.9:g.14375510_14375513dup	NC_000021.9:g.14375509_14375513dup	NC_000021.9:g.14375508_14375513dup	NC_000021.9:g.14375507_14375513dup	NC_000021.9:g.14375505_14375513dup	NC_000021.9:g.14375503_14375513dup
GRCh37.p13 chr 21	NC_000021.8:g.15747813_15747834=	NC_000021.8:g.15747823_15747834del	NC_000021.8:g.15747827_15747834del	NC_000021.8:g.15747829_15747834del	NC_000021.8:g.15747830_15747834del	NC_000021.8:g.15747831_15747834del	NC_000021.8:g.15747832_15747834del	NC_000021.8:g.15747833_15747834del	NC_000021.8:g.15747834del	NC_000021.8:g.15747834dup	NC_000021.8:g.15747833_15747834dup	NC_000021.8:g.15747832_15747834dup	NC_000021.8:g.15747831_15747834dup	NC_000021.8:g.15747830_15747834dup	NC_000021.8:g.15747829_15747834dup	NC_000021.8:g.15747828_15747834dup	NC_000021.8:g.15747826_15747834dup	NC_000021.8:g.15747824_15747834dup
HSPA13 transcript	NM_006948.4:c.748+160=	NM_006948.4:c.748+149_748+160del	NM_006948.4:c.748+153_748+160del	NM_006948.4:c.748+155_748+160del	NM_006948.4:c.748+156_748+160del	NM_006948.4:c.748+157_748+160del	NM_006948.4:c.748+158_748+160del	NM_006948.4:c.748+159_748+160del	NM_006948.4:c.748+160del	NM_006948.4:c.748+160dup	NM_006948.4:c.748+159_748+160dup	NM_006948.4:c.748+158_748+160dup	NM_006948.4:c.748+157_748+160dup	NM_006948.4:c.748+156_748+160dup	NM_006948.4:c.748+155_748+160dup	NM_006948.4:c.748+154_748+160dup	NM_006948.4:c.748+152_748+160dup	NM_006948.4:c.748+150_748+160dup
HSPA13 transcript	NM_006948.5:c.748+160=	NM_006948.5:c.748+149_748+160del	NM_006948.5:c.748+153_748+160del	NM_006948.5:c.748+155_748+160del	NM_006948.5:c.748+156_748+160del	NM_006948.5:c.748+157_748+160del	NM_006948.5:c.748+158_748+160del	NM_006948.5:c.748+159_748+160del	NM_006948.5:c.748+160del	NM_006948.5:c.748+160dup	NM_006948.5:c.748+159_748+160dup	NM_006948.5:c.748+158_748+160dup	NM_006948.5:c.748+157_748+160dup	NM_006948.5:c.748+156_748+160dup	NM_006948.5:c.748+155_748+160dup	NM_006948.5:c.748+154_748+160dup	NM_006948.5:c.748+152_748+160dup	NM_006948.5:c.748+150_748+160dup
HSPA13 transcript variant X1	XM_005261036.1:c.124+160=	XM_005261036.1:c.124+149_124+160del	XM_005261036.1:c.124+153_124+160del	XM_005261036.1:c.124+155_124+160del	XM_005261036.1:c.124+156_124+160del	XM_005261036.1:c.124+157_124+160del	XM_005261036.1:c.124+158_124+160del	XM_005261036.1:c.124+159_124+160del	XM_005261036.1:c.124+160del	XM_005261036.1:c.124+160dup	XM_005261036.1:c.124+159_124+160dup	XM_005261036.1:c.124+158_124+160dup	XM_005261036.1:c.124+157_124+160dup	XM_005261036.1:c.124+156_124+160dup	XM_005261036.1:c.124+155_124+160dup	XM_005261036.1:c.124+154_124+160dup	XM_005261036.1:c.124+152_124+160dup	XM_005261036.1:c.124+150_124+160dup

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#.

75 SubSNP, 43 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss41448880	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95745473	Feb 05, 2009 (130)
3	HUMANGENOME_JCVI	ss96175794	Mar 15, 2016 (147)
4	PJP	ss295059459	Aug 21, 2014 (142)
5	1000GENOMES	ss1378643408	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1709432830	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1709433412	Apr 01, 2015 (144)
8	EVA_UK10K_ALSPAC	ss1710823326	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710823329	Apr 01, 2015 (144)
10	SWEGEN	ss3018606133	Nov 08, 2017 (151)
11	URBANLAB	ss3651074709	Oct 12, 2018 (152)
12	EVA_DECODE	ss3707380892	Jul 13, 2019 (153)
13	EVA_DECODE	ss3707380893	Jul 13, 2019 (153)
14	EVA_DECODE	ss3707380894	Jul 13, 2019 (153)
15	EVA_DECODE	ss3707380895	Jul 13, 2019 (153)
16	EVA_DECODE	ss3707380896	Jul 13, 2019 (153)
17	EVA_DECODE	ss3707380897	Jul 13, 2019 (153)
18	ACPOP	ss3743571047	Jul 13, 2019 (153)
19	ACPOP	ss3743571048	Jul 13, 2019 (153)
20	ACPOP	ss3743571049	Jul 13, 2019 (153)
21	ACPOP	ss3743571050	Jul 13, 2019 (153)
22	PACBIO	ss3793592969	Jul 13, 2019 (153)
23	PACBIO	ss3793592970	Jul 13, 2019 (153)
24	PACBIO	ss3798479099	Jul 13, 2019 (153)
25	PACBIO	ss3798479100	Jul 13, 2019 (153)
26	KHV_HUMAN_GENOMES	ss3822049743	Jul 13, 2019 (153)
27	EVA	ss3835775829	Apr 27, 2020 (154)
28	KOGIC	ss3982781909	Apr 27, 2020 (154)
29	KOGIC	ss3982781910	Apr 27, 2020 (154)
30	KOGIC	ss3982781911	Apr 27, 2020 (154)
31	KOGIC	ss3982781912	Apr 27, 2020 (154)
32	KOGIC	ss3982781913	Apr 27, 2020 (154)
33	KOGIC	ss3982781914	Apr 27, 2020 (154)
34	GNOMAD	ss4357362252	Apr 26, 2021 (155)
35	GNOMAD	ss4357362253	Apr 26, 2021 (155)
36	GNOMAD	ss4357362254	Apr 26, 2021 (155)
37	GNOMAD	ss4357362255	Apr 26, 2021 (155)
38	GNOMAD	ss4357362256	Apr 26, 2021 (155)
39	GNOMAD	ss4357362257	Apr 26, 2021 (155)
40	GNOMAD	ss4357362258	Apr 26, 2021 (155)
41	GNOMAD	ss4357362259	Apr 26, 2021 (155)
42	GNOMAD	ss4357362261	Apr 26, 2021 (155)
43	GNOMAD	ss4357362262	Apr 26, 2021 (155)
44	GNOMAD	ss4357362263	Apr 26, 2021 (155)
45	GNOMAD	ss4357362264	Apr 26, 2021 (155)
46	GNOMAD	ss4357362265	Apr 26, 2021 (155)
47	GNOMAD	ss4357362266	Apr 26, 2021 (155)
48	GNOMAD	ss4357362267	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5230751647	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5230751648	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5230751649	Apr 26, 2021 (155)
52	TOMMO_GENOMICS	ss5230751650	Apr 26, 2021 (155)
53	TOMMO_GENOMICS	ss5230751651	Apr 26, 2021 (155)
54	TOMMO_GENOMICS	ss5230751652	Apr 26, 2021 (155)
55	1000G_HIGH_COVERAGE	ss5309598213	Oct 13, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5309598214	Oct 13, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5309598215	Oct 13, 2022 (156)
58	1000G_HIGH_COVERAGE	ss5309598216	Oct 13, 2022 (156)
59	1000G_HIGH_COVERAGE	ss5309598217	Oct 13, 2022 (156)
60	1000G_HIGH_COVERAGE	ss5309598218	Oct 13, 2022 (156)
61	HUGCELL_USP	ss5501701935	Oct 13, 2022 (156)
62	HUGCELL_USP	ss5501701936	Oct 13, 2022 (156)
63	HUGCELL_USP	ss5501701937	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5501701938	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5501701939	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5501701940	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5791051050	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5791051051	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5791051052	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5791051053	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5791051054	Oct 13, 2022 (156)
72	TOMMO_GENOMICS	ss5791051055	Oct 13, 2022 (156)
73	EVA	ss5838799066	Oct 13, 2022 (156)
74	EVA	ss5838799067	Oct 13, 2022 (156)
75	EVA	ss5853223222	Oct 13, 2022 (156)
76	1000Genomes	NC_000021.8 - 15747813	Oct 12, 2018 (152)
77	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43755590 (NC_000021.8:15747813:T: 2172/3854) Row 43755591 (NC_000021.8:15747812:TTT: 936/3854)	-	Oct 12, 2018 (152)
78	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 43755590 (NC_000021.8:15747813:T: 2172/3854) Row 43755591 (NC_000021.8:15747812:TTT: 936/3854)	-	Oct 12, 2018 (152)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 558227282 (NC_000021.9:14375491::T 744/117962) Row 558227283 (NC_000021.9:14375491::TT 1511/117950) Row 558227284 (NC_000021.9:14375491::TTT 15421/117614)...	-	Apr 26, 2021 (155)
94	Korean Genome Project Submission ignored due to conflicting rows: Row 39159910 (NC_000021.9:14375493:T: 152/1832) Row 39159911 (NC_000021.9:14375494::T 79/1832) Row 39159912 (NC_000021.9:14375491:TTT: 88/1832)...	-	Apr 27, 2020 (154)
95	Korean Genome Project Submission ignored due to conflicting rows: Row 39159910 (NC_000021.9:14375493:T: 152/1832) Row 39159911 (NC_000021.9:14375494::T 79/1832) Row 39159912 (NC_000021.9:14375491:TTT: 88/1832)...	-	Apr 27, 2020 (154)
96	Korean Genome Project Submission ignored due to conflicting rows: Row 39159910 (NC_000021.9:14375493:T: 152/1832) Row 39159911 (NC_000021.9:14375494::T 79/1832) Row 39159912 (NC_000021.9:14375491:TTT: 88/1832)...	-	Apr 27, 2020 (154)
97	Korean Genome Project Submission ignored due to conflicting rows: Row 39159910 (NC_000021.9:14375493:T: 152/1832) Row 39159911 (NC_000021.9:14375494::T 79/1832) Row 39159912 (NC_000021.9:14375491:TTT: 88/1832)...	-	Apr 27, 2020 (154)
98	Korean Genome Project Submission ignored due to conflicting rows: Row 39159910 (NC_000021.9:14375493:T: 152/1832) Row 39159911 (NC_000021.9:14375494::T 79/1832) Row 39159912 (NC_000021.9:14375491:TTT: 88/1832)...	-	Apr 27, 2020 (154)
99	Korean Genome Project Submission ignored due to conflicting rows: Row 39159910 (NC_000021.9:14375493:T: 152/1832) Row 39159911 (NC_000021.9:14375494::T 79/1832) Row 39159912 (NC_000021.9:14375491:TTT: 88/1832)...	-	Apr 27, 2020 (154)
100	Northern Sweden Submission ignored due to conflicting rows: Row 16855912 (NC_000021.8:15747812:TT: 116/598) Row 16855913 (NC_000021.8:15747812:TTT: 9/598) Row 16855914 (NC_000021.8:15747812:T: 55/598)...	-	Jul 13, 2019 (153)
101	Northern Sweden Submission ignored due to conflicting rows: Row 16855912 (NC_000021.8:15747812:TT: 116/598) Row 16855913 (NC_000021.8:15747812:TTT: 9/598) Row 16855914 (NC_000021.8:15747812:T: 55/598)...	-	Jul 13, 2019 (153)
102	Northern Sweden Submission ignored due to conflicting rows: Row 16855912 (NC_000021.8:15747812:TT: 116/598) Row 16855913 (NC_000021.8:15747812:TTT: 9/598) Row 16855914 (NC_000021.8:15747812:T: 55/598)...	-	Jul 13, 2019 (153)
103	Northern Sweden Submission ignored due to conflicting rows: Row 16855912 (NC_000021.8:15747812:TT: 116/598) Row 16855913 (NC_000021.8:15747812:TTT: 9/598) Row 16855914 (NC_000021.8:15747812:T: 55/598)...	-	Jul 13, 2019 (153)
104	8.3KJPN Submission ignored due to conflicting rows: Row 88720954 (NC_000021.8:15747812:TT: 5523/16728) Row 88720955 (NC_000021.8:15747812::TTT 1321/16728) Row 88720956 (NC_000021.8:15747812::T 108/16728)...	-	Apr 26, 2021 (155)
105	8.3KJPN Submission ignored due to conflicting rows: Row 88720954 (NC_000021.8:15747812:TT: 5523/16728) Row 88720955 (NC_000021.8:15747812::TTT 1321/16728) Row 88720956 (NC_000021.8:15747812::T 108/16728)...	-	Apr 26, 2021 (155)
106	8.3KJPN Submission ignored due to conflicting rows: Row 88720954 (NC_000021.8:15747812:TT: 5523/16728) Row 88720955 (NC_000021.8:15747812::TTT 1321/16728) Row 88720956 (NC_000021.8:15747812::T 108/16728)...	-	Apr 26, 2021 (155)
107	8.3KJPN Submission ignored due to conflicting rows: Row 88720954 (NC_000021.8:15747812:TT: 5523/16728) Row 88720955 (NC_000021.8:15747812::TTT 1321/16728) Row 88720956 (NC_000021.8:15747812::T 108/16728)...	-	Apr 26, 2021 (155)
108	8.3KJPN Submission ignored due to conflicting rows: Row 88720954 (NC_000021.8:15747812:TT: 5523/16728) Row 88720955 (NC_000021.8:15747812::TTT 1321/16728) Row 88720956 (NC_000021.8:15747812::T 108/16728)...	-	Apr 26, 2021 (155)
109	8.3KJPN Submission ignored due to conflicting rows: Row 88720954 (NC_000021.8:15747812:TT: 5523/16728) Row 88720955 (NC_000021.8:15747812::TTT 1321/16728) Row 88720956 (NC_000021.8:15747812::T 108/16728)...	-	Apr 26, 2021 (155)
110	14KJPN Submission ignored due to conflicting rows: Row 124888154 (NC_000021.9:14375491:TT: 9588/28250) Row 124888155 (NC_000021.9:14375491::TTT 2248/28250) Row 124888156 (NC_000021.9:14375491:TTT: 216/28250)...	-	Oct 13, 2022 (156)
111	14KJPN Submission ignored due to conflicting rows: Row 124888154 (NC_000021.9:14375491:TT: 9588/28250) Row 124888155 (NC_000021.9:14375491::TTT 2248/28250) Row 124888156 (NC_000021.9:14375491:TTT: 216/28250)...	-	Oct 13, 2022 (156)
112	14KJPN Submission ignored due to conflicting rows: Row 124888154 (NC_000021.9:14375491:TT: 9588/28250) Row 124888155 (NC_000021.9:14375491::TTT 2248/28250) Row 124888156 (NC_000021.9:14375491:TTT: 216/28250)...	-	Oct 13, 2022 (156)
113	14KJPN Submission ignored due to conflicting rows: Row 124888154 (NC_000021.9:14375491:TT: 9588/28250) Row 124888155 (NC_000021.9:14375491::TTT 2248/28250) Row 124888156 (NC_000021.9:14375491:TTT: 216/28250)...	-	Oct 13, 2022 (156)
114	14KJPN Submission ignored due to conflicting rows: Row 124888154 (NC_000021.9:14375491:TT: 9588/28250) Row 124888155 (NC_000021.9:14375491::TTT 2248/28250) Row 124888156 (NC_000021.9:14375491:TTT: 216/28250)...	-	Oct 13, 2022 (156)
115	14KJPN Submission ignored due to conflicting rows: Row 124888154 (NC_000021.9:14375491:TT: 9588/28250) Row 124888155 (NC_000021.9:14375491::TTT 2248/28250) Row 124888156 (NC_000021.9:14375491:TTT: 216/28250)...	-	Oct 13, 2022 (156)
116	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43755590 (NC_000021.8:15747813:T: 2101/3708) Row 43755591 (NC_000021.8:15747812:TTT: 894/3708)	-	Oct 12, 2018 (152)
117	UK 10K study - Twins Submission ignored due to conflicting rows: Row 43755590 (NC_000021.8:15747813:T: 2101/3708) Row 43755591 (NC_000021.8:15747812:TTT: 894/3708)	-	Oct 12, 2018 (152)
118	ALFA	NC_000021.9 - 14375492	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
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4357362267	NC_000021.9:14375491:TTTTTTTT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4357362266	NC_000021.9:14375491:TTTTTT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4357362265	NC_000021.9:14375491:TTTTT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4357362264	NC_000021.9:14375491:TTTT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss1709432830, ss1709433412, ss3018606133, ss3743571048, ss5230751650, ss5838799067	NC_000021.8:15747812:TTT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3707380892, ss3982781911, ss4357362263, ss5309598215, ss5501701938, ss5791051052	NC_000021.9:14375491:TTT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss295059459	NC_000021.7:14669683:TT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
79077150, ss1378643408, ss3743571047, ss3835775829, ss5230751647, ss5838799066	NC_000021.8:15747812:TT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1710823326, ss1710823329	NC_000021.8:15747813:TT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3822049743, ss4357362262, ss5309598213, ss5501701940, ss5791051050	NC_000021.9:14375491:TT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3707380893, ss3982781912	NC_000021.9:14375492:TT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss96175794	NT_011512.11:1409683:TT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss41448880, ss95745473	NT_011512.11:1409703:TT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3743571049, ss5230751651	NC_000021.8:15747812:T:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000021.8:15747813:T:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3651074709, ss4357362261, ss5309598216, ss5501701939, ss5791051053	NC_000021.9:14375491:T:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3707380894, ss3982781909	NC_000021.9:14375493:T:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5230751649	NC_000021.8:15747812::T	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362252, ss5791051054	NC_000021.9:14375491::T	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3982781910	NC_000021.9:14375494::T	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3793592969, ss3798479099, ss5230751652	NC_000021.8:15747812::TT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362253, ss5309598218, ss5501701935	NC_000021.9:14375491::TT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3982781914	NC_000021.9:14375494::TT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3743571050, ss3793592970, ss3798479100, ss5230751648	NC_000021.8:15747812::TTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362254, ss5309598214, ss5501701936, ss5791051051, ss5853223222	NC_000021.9:14375491::TTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3707380895, ss3982781913	NC_000021.9:14375494::TTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362255, ss5309598217, ss5501701937, ss5791051055	NC_000021.9:14375491::TTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3707380896	NC_000021.9:14375494::TTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362256	NC_000021.9:14375491::TTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362257	NC_000021.9:14375491::TTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
13909552871	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362258	NC_000021.9:14375491::TTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4357362259	NC_000021.9:14375491::TTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3707380897	NC_000021.9:14375494::TTTTTTTTTTT	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss2410931428	NC_000021.8:15747812:TTTTTTTT:	NC_000021.9:14375491:TTTTTTTTTTTTT… NC_000021.9:14375491:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

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

No publications for rs34202425

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

rs34202425