Name: rs34005167
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.

rs34005167

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr12:111874774-111874792 (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)₉ / del(T)₇ / del(T)₅ / del(…
del(T)₉ / del(T)₇ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dup(T)₄ / dup(T)₈
Variation Type: Indel Insertion and Deletion
Frequency: delTT=0.03661 (419/11446, ALFA)
delTT=0.017 (10/598, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAPKAPK5 : 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	11446	TTTTTTTTTTTTTTTTTTT=0.96034	TTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00017, TTTTTTTTTTTTTTTTT=0.03661, TTTTTTTTTTTTTTTTTTTT=0.00210, TTTTTTTTTTTTTTTTTT=0.00061, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00017, TTTTTTTTTTTTTTTTTTTTT=0.00000	0.931295	0.004217	0.064488	21
European	Sub	9756	TTTTTTTTTTTTTTTTTTT=0.9536	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTT=0.0428, TTTTTTTTTTTTTTTTTTTT=0.0025, TTTTTTTTTTTTTTTTTT=0.0007, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0002, TTTTTTTTTTTTTTTTTTTTT=0.0000	0.919521	0.004953	0.075526	16
African	Sub	1042	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	40	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1002	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
East Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	78	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	264	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	50	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	256	TTTTTTTTTTTTTTTTTTT=0.996	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	0.992188	0.0	0.007812	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	11446	(T)₁₉=0.96034	del(T)₉=0.00000, del(T)₇=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00017, delTT=0.03661, delT=0.00061, dupT=0.00210, dupTT=0.00000, dup(T)₈=0.00017
Allele Frequency Aggregator	European	Sub	9756	(T)₁₉=0.9536	del(T)₉=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0002, delTT=0.0428, delT=0.0007, dupT=0.0025, dupTT=0.0000, dup(T)₈=0.0002
Allele Frequency Aggregator	African	Sub	1042	(T)₁₉=1.0000	del(T)₉=0.0000, del(T)₇=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₈=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	264	(T)₁₉=1.000	del(T)₉=0.000, del(T)₇=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, dup(T)₈=0.000
Allele Frequency Aggregator	Other	Sub	256	(T)₁₉=0.996	del(T)₉=0.000, del(T)₇=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.004, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₈=0.000
Allele Frequency Aggregator	Latin American 1	Sub	78	(T)₁₉=1.00	del(T)₉=0.00, del(T)₇=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, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	50	(T)₁₉=1.00	del(T)₉=0.00, del(T)₇=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, dup(T)₈=0.00
Allele Frequency Aggregator	Asian	Sub	0	(T)₁₉=0	del(T)₉=0, del(T)₇=0, del(T)₅=0, del(T)₄=0, delTTT=0, delTT=0, delT=0, dupT=0, dupTT=0, dup(T)₈=0
Northern Sweden	ACPOP	Study-wide	598	(T)₁₉=0.983	delTT=0.017

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 12	NC_000012.12:g.111874784_111874792del
GRCh38.p14 chr 12	NC_000012.12:g.111874786_111874792del
GRCh38.p14 chr 12	NC_000012.12:g.111874788_111874792del
GRCh38.p14 chr 12	NC_000012.12:g.111874789_111874792del
GRCh38.p14 chr 12	NC_000012.12:g.111874790_111874792del
GRCh38.p14 chr 12	NC_000012.12:g.111874791_111874792del
GRCh38.p14 chr 12	NC_000012.12:g.111874792del
GRCh38.p14 chr 12	NC_000012.12:g.111874792dup
GRCh38.p14 chr 12	NC_000012.12:g.111874791_111874792dup
GRCh38.p14 chr 12	NC_000012.12:g.111874789_111874792dup
GRCh38.p14 chr 12	NC_000012.12:g.111874785_111874792dup
GRCh37.p13 chr 12	NC_000012.11:g.112312588_112312596del
GRCh37.p13 chr 12	NC_000012.11:g.112312590_112312596del
GRCh37.p13 chr 12	NC_000012.11:g.112312592_112312596del
GRCh37.p13 chr 12	NC_000012.11:g.112312593_112312596del
GRCh37.p13 chr 12	NC_000012.11:g.112312594_112312596del
GRCh37.p13 chr 12	NC_000012.11:g.112312595_112312596del
GRCh37.p13 chr 12	NC_000012.11:g.112312596del
GRCh37.p13 chr 12	NC_000012.11:g.112312596dup
GRCh37.p13 chr 12	NC_000012.11:g.112312595_112312596dup
GRCh37.p13 chr 12	NC_000012.11:g.112312593_112312596dup
GRCh37.p13 chr 12	NC_000012.11:g.112312589_112312596dup

Gene: MAPKAPK5, MAPK activated protein kinase 5 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAPKAPK5 transcript variant 3	NM_001371479.1:c.579+3604… NM_001371479.1:c.579+3604_579+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 4	NM_001371480.1:c.579+3604… NM_001371480.1:c.579+3604_579+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 5	NM_001371481.1:c.579+3604… NM_001371481.1:c.579+3604_579+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 6	NM_001371482.1:c.489+3604… NM_001371482.1:c.489+3604_489+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 7	NM_001371483.1:c.489+3604… NM_001371483.1:c.489+3604_489+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 8	NM_001371484.1:c.477+3604… NM_001371484.1:c.477+3604_477+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 9	NM_001371485.1:c.372+3604… NM_001371485.1:c.372+3604_372+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 10	NM_001371486.1:c.372+3604… NM_001371486.1:c.372+3604_372+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 11	NM_001371487.1:c.282+3604… NM_001371487.1:c.282+3604_282+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 1	NM_003668.4:c.579+3604_57… NM_003668.4:c.579+3604_579+3612del	N/A	Intron Variant
MAPKAPK5 transcript variant 2	NM_139078.3:c.579+3604_57… NM_139078.3:c.579+3604_579+3612del	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)₁₉=	del(T)₉	del(T)₇	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dup(T)₄	dup(T)₈
GRCh38.p14 chr 12	NC_000012.12:g.111874774_111874792=	NC_000012.12:g.111874784_111874792del	NC_000012.12:g.111874786_111874792del	NC_000012.12:g.111874788_111874792del	NC_000012.12:g.111874789_111874792del	NC_000012.12:g.111874790_111874792del	NC_000012.12:g.111874791_111874792del	NC_000012.12:g.111874792del	NC_000012.12:g.111874792dup	NC_000012.12:g.111874791_111874792dup	NC_000012.12:g.111874789_111874792dup	NC_000012.12:g.111874785_111874792dup
GRCh37.p13 chr 12	NC_000012.11:g.112312578_112312596=	NC_000012.11:g.112312588_112312596del	NC_000012.11:g.112312590_112312596del	NC_000012.11:g.112312592_112312596del	NC_000012.11:g.112312593_112312596del	NC_000012.11:g.112312594_112312596del	NC_000012.11:g.112312595_112312596del	NC_000012.11:g.112312596del	NC_000012.11:g.112312596dup	NC_000012.11:g.112312595_112312596dup	NC_000012.11:g.112312593_112312596dup	NC_000012.11:g.112312589_112312596dup
MAPKAPK5 transcript variant 3	NM_001371479.1:c.579+3594=	NM_001371479.1:c.579+3604_579+3612del	NM_001371479.1:c.579+3606_579+3612del	NM_001371479.1:c.579+3608_579+3612del	NM_001371479.1:c.579+3609_579+3612del	NM_001371479.1:c.579+3610_579+3612del	NM_001371479.1:c.579+3611_579+3612del	NM_001371479.1:c.579+3612del	NM_001371479.1:c.579+3612dup	NM_001371479.1:c.579+3611_579+3612dup	NM_001371479.1:c.579+3609_579+3612dup	NM_001371479.1:c.579+3605_579+3612dup
MAPKAPK5 transcript variant 4	NM_001371480.1:c.579+3594=	NM_001371480.1:c.579+3604_579+3612del	NM_001371480.1:c.579+3606_579+3612del	NM_001371480.1:c.579+3608_579+3612del	NM_001371480.1:c.579+3609_579+3612del	NM_001371480.1:c.579+3610_579+3612del	NM_001371480.1:c.579+3611_579+3612del	NM_001371480.1:c.579+3612del	NM_001371480.1:c.579+3612dup	NM_001371480.1:c.579+3611_579+3612dup	NM_001371480.1:c.579+3609_579+3612dup	NM_001371480.1:c.579+3605_579+3612dup
MAPKAPK5 transcript variant 5	NM_001371481.1:c.579+3594=	NM_001371481.1:c.579+3604_579+3612del	NM_001371481.1:c.579+3606_579+3612del	NM_001371481.1:c.579+3608_579+3612del	NM_001371481.1:c.579+3609_579+3612del	NM_001371481.1:c.579+3610_579+3612del	NM_001371481.1:c.579+3611_579+3612del	NM_001371481.1:c.579+3612del	NM_001371481.1:c.579+3612dup	NM_001371481.1:c.579+3611_579+3612dup	NM_001371481.1:c.579+3609_579+3612dup	NM_001371481.1:c.579+3605_579+3612dup
MAPKAPK5 transcript variant 6	NM_001371482.1:c.489+3594=	NM_001371482.1:c.489+3604_489+3612del	NM_001371482.1:c.489+3606_489+3612del	NM_001371482.1:c.489+3608_489+3612del	NM_001371482.1:c.489+3609_489+3612del	NM_001371482.1:c.489+3610_489+3612del	NM_001371482.1:c.489+3611_489+3612del	NM_001371482.1:c.489+3612del	NM_001371482.1:c.489+3612dup	NM_001371482.1:c.489+3611_489+3612dup	NM_001371482.1:c.489+3609_489+3612dup	NM_001371482.1:c.489+3605_489+3612dup
MAPKAPK5 transcript variant 7	NM_001371483.1:c.489+3594=	NM_001371483.1:c.489+3604_489+3612del	NM_001371483.1:c.489+3606_489+3612del	NM_001371483.1:c.489+3608_489+3612del	NM_001371483.1:c.489+3609_489+3612del	NM_001371483.1:c.489+3610_489+3612del	NM_001371483.1:c.489+3611_489+3612del	NM_001371483.1:c.489+3612del	NM_001371483.1:c.489+3612dup	NM_001371483.1:c.489+3611_489+3612dup	NM_001371483.1:c.489+3609_489+3612dup	NM_001371483.1:c.489+3605_489+3612dup
MAPKAPK5 transcript variant 8	NM_001371484.1:c.477+3594=	NM_001371484.1:c.477+3604_477+3612del	NM_001371484.1:c.477+3606_477+3612del	NM_001371484.1:c.477+3608_477+3612del	NM_001371484.1:c.477+3609_477+3612del	NM_001371484.1:c.477+3610_477+3612del	NM_001371484.1:c.477+3611_477+3612del	NM_001371484.1:c.477+3612del	NM_001371484.1:c.477+3612dup	NM_001371484.1:c.477+3611_477+3612dup	NM_001371484.1:c.477+3609_477+3612dup	NM_001371484.1:c.477+3605_477+3612dup
MAPKAPK5 transcript variant 9	NM_001371485.1:c.372+3594=	NM_001371485.1:c.372+3604_372+3612del	NM_001371485.1:c.372+3606_372+3612del	NM_001371485.1:c.372+3608_372+3612del	NM_001371485.1:c.372+3609_372+3612del	NM_001371485.1:c.372+3610_372+3612del	NM_001371485.1:c.372+3611_372+3612del	NM_001371485.1:c.372+3612del	NM_001371485.1:c.372+3612dup	NM_001371485.1:c.372+3611_372+3612dup	NM_001371485.1:c.372+3609_372+3612dup	NM_001371485.1:c.372+3605_372+3612dup
MAPKAPK5 transcript variant 10	NM_001371486.1:c.372+3594=	NM_001371486.1:c.372+3604_372+3612del	NM_001371486.1:c.372+3606_372+3612del	NM_001371486.1:c.372+3608_372+3612del	NM_001371486.1:c.372+3609_372+3612del	NM_001371486.1:c.372+3610_372+3612del	NM_001371486.1:c.372+3611_372+3612del	NM_001371486.1:c.372+3612del	NM_001371486.1:c.372+3612dup	NM_001371486.1:c.372+3611_372+3612dup	NM_001371486.1:c.372+3609_372+3612dup	NM_001371486.1:c.372+3605_372+3612dup
MAPKAPK5 transcript variant 11	NM_001371487.1:c.282+3594=	NM_001371487.1:c.282+3604_282+3612del	NM_001371487.1:c.282+3606_282+3612del	NM_001371487.1:c.282+3608_282+3612del	NM_001371487.1:c.282+3609_282+3612del	NM_001371487.1:c.282+3610_282+3612del	NM_001371487.1:c.282+3611_282+3612del	NM_001371487.1:c.282+3612del	NM_001371487.1:c.282+3612dup	NM_001371487.1:c.282+3611_282+3612dup	NM_001371487.1:c.282+3609_282+3612dup	NM_001371487.1:c.282+3605_282+3612dup
MAPKAPK5 transcript variant 1	NM_003668.3:c.579+3594=	NM_003668.3:c.579+3604_579+3612del	NM_003668.3:c.579+3606_579+3612del	NM_003668.3:c.579+3608_579+3612del	NM_003668.3:c.579+3609_579+3612del	NM_003668.3:c.579+3610_579+3612del	NM_003668.3:c.579+3611_579+3612del	NM_003668.3:c.579+3612del	NM_003668.3:c.579+3612dup	NM_003668.3:c.579+3611_579+3612dup	NM_003668.3:c.579+3609_579+3612dup	NM_003668.3:c.579+3605_579+3612dup
MAPKAPK5 transcript variant 1	NM_003668.4:c.579+3594=	NM_003668.4:c.579+3604_579+3612del	NM_003668.4:c.579+3606_579+3612del	NM_003668.4:c.579+3608_579+3612del	NM_003668.4:c.579+3609_579+3612del	NM_003668.4:c.579+3610_579+3612del	NM_003668.4:c.579+3611_579+3612del	NM_003668.4:c.579+3612del	NM_003668.4:c.579+3612dup	NM_003668.4:c.579+3611_579+3612dup	NM_003668.4:c.579+3609_579+3612dup	NM_003668.4:c.579+3605_579+3612dup
MAPKAPK5 transcript variant 2	NM_139078.2:c.579+3594=	NM_139078.2:c.579+3604_579+3612del	NM_139078.2:c.579+3606_579+3612del	NM_139078.2:c.579+3608_579+3612del	NM_139078.2:c.579+3609_579+3612del	NM_139078.2:c.579+3610_579+3612del	NM_139078.2:c.579+3611_579+3612del	NM_139078.2:c.579+3612del	NM_139078.2:c.579+3612dup	NM_139078.2:c.579+3611_579+3612dup	NM_139078.2:c.579+3609_579+3612dup	NM_139078.2:c.579+3605_579+3612dup
MAPKAPK5 transcript variant 2	NM_139078.3:c.579+3594=	NM_139078.3:c.579+3604_579+3612del	NM_139078.3:c.579+3606_579+3612del	NM_139078.3:c.579+3608_579+3612del	NM_139078.3:c.579+3609_579+3612del	NM_139078.3:c.579+3610_579+3612del	NM_139078.3:c.579+3611_579+3612del	NM_139078.3:c.579+3612del	NM_139078.3:c.579+3612dup	NM_139078.3:c.579+3611_579+3612dup	NM_139078.3:c.579+3609_579+3612dup	NM_139078.3:c.579+3605_579+3612dup
MAPKAPK5 transcript variant X1	XM_005253974.1:c.489+3594=	XM_005253974.1:c.489+3604_489+3612del	XM_005253974.1:c.489+3606_489+3612del	XM_005253974.1:c.489+3608_489+3612del	XM_005253974.1:c.489+3609_489+3612del	XM_005253974.1:c.489+3610_489+3612del	XM_005253974.1:c.489+3611_489+3612del	XM_005253974.1:c.489+3612del	XM_005253974.1:c.489+3612dup	XM_005253974.1:c.489+3611_489+3612dup	XM_005253974.1:c.489+3609_489+3612dup	XM_005253974.1:c.489+3605_489+3612dup
MAPKAPK5 transcript variant X2	XM_005253975.1:c.372+3594=	XM_005253975.1:c.372+3604_372+3612del	XM_005253975.1:c.372+3606_372+3612del	XM_005253975.1:c.372+3608_372+3612del	XM_005253975.1:c.372+3609_372+3612del	XM_005253975.1:c.372+3610_372+3612del	XM_005253975.1:c.372+3611_372+3612del	XM_005253975.1:c.372+3612del	XM_005253975.1:c.372+3612dup	XM_005253975.1:c.372+3611_372+3612dup	XM_005253975.1:c.372+3609_372+3612dup	XM_005253975.1:c.372+3605_372+3612dup
MAPKAPK5 transcript variant X3	XM_005253976.1:c.300+3594=	XM_005253976.1:c.300+3604_300+3612del	XM_005253976.1:c.300+3606_300+3612del	XM_005253976.1:c.300+3608_300+3612del	XM_005253976.1:c.300+3609_300+3612del	XM_005253976.1:c.300+3610_300+3612del	XM_005253976.1:c.300+3611_300+3612del	XM_005253976.1:c.300+3612del	XM_005253976.1:c.300+3612dup	XM_005253976.1:c.300+3611_300+3612dup	XM_005253976.1:c.300+3609_300+3612dup	XM_005253976.1:c.300+3605_300+3612dup
MAPKAPK5 transcript variant X4	XM_005253977.1:c.39+3594=	XM_005253977.1:c.39+3604_39+3612del	XM_005253977.1:c.39+3606_39+3612del	XM_005253977.1:c.39+3608_39+3612del	XM_005253977.1:c.39+3609_39+3612del	XM_005253977.1:c.39+3610_39+3612del	XM_005253977.1:c.39+3611_39+3612del	XM_005253977.1:c.39+3612del	XM_005253977.1:c.39+3612dup	XM_005253977.1:c.39+3611_39+3612dup	XM_005253977.1:c.39+3609_39+3612dup	XM_005253977.1:c.39+3605_39+3612dup
MAPKAPK5 transcript variant X5	XM_005253978.1:c.39+3594=	XM_005253978.1:c.39+3604_39+3612del	XM_005253978.1:c.39+3606_39+3612del	XM_005253978.1:c.39+3608_39+3612del	XM_005253978.1:c.39+3609_39+3612del	XM_005253978.1:c.39+3610_39+3612del	XM_005253978.1:c.39+3611_39+3612del	XM_005253978.1:c.39+3612del	XM_005253978.1:c.39+3612dup	XM_005253978.1:c.39+3611_39+3612dup	XM_005253978.1:c.39+3609_39+3612dup	XM_005253978.1:c.39+3605_39+3612dup
MAPKAPK5 transcript variant X6	XM_005253979.1:c.-185+3594=	XM_005253979.1:c.-185+3604_-185+3612del	XM_005253979.1:c.-185+3606_-185+3612del	XM_005253979.1:c.-185+3608_-185+3612del	XM_005253979.1:c.-185+3609_-185+3612del	XM_005253979.1:c.-185+3610_-185+3612del	XM_005253979.1:c.-185+3611_-185+3612del	XM_005253979.1:c.-185+3612del	XM_005253979.1:c.-185+3612dup	XM_005253979.1:c.-185+3611_-185+3612dup	XM_005253979.1:c.-185+3609_-185+3612dup	XM_005253979.1:c.-185+3605_-185+3612dup

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#.

43 SubSNP, 17 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40129020	Dec 03, 2013 (138)
2	ABI	ss40220268	Mar 13, 2006 (126)
3	HGSV	ss79902288	Dec 14, 2007 (137)
4	HGSV	ss80106706	Dec 14, 2007 (137)
5	PJP	ss294774751	May 09, 2011 (134)
6	PJP	ss294774752	May 09, 2011 (137)
7	SWEGEN	ss3010358590	Nov 08, 2017 (151)
8	MCHAISSO	ss3064576166	Nov 08, 2017 (151)
9	MCHAISSO	ss3065497890	Nov 08, 2017 (151)
10	EVA_DECODE	ss3694478218	Jul 13, 2019 (153)
11	EVA_DECODE	ss3694478219	Jul 13, 2019 (153)
12	EVA_DECODE	ss3694478220	Jul 13, 2019 (153)
13	EVA_DECODE	ss3694478221	Jul 13, 2019 (153)
14	ACPOP	ss3739387196	Jul 13, 2019 (153)
15	PACBIO	ss3787337513	Jul 13, 2019 (153)
16	PACBIO	ss3792419559	Jul 13, 2019 (153)
17	PACBIO	ss3797302643	Jul 13, 2019 (153)
18	EVA	ss3833328931	Apr 27, 2020 (154)
19	GNOMAD	ss4259130827	Apr 27, 2021 (155)
20	GNOMAD	ss4259130828	Apr 27, 2021 (155)
21	GNOMAD	ss4259130829	Apr 27, 2021 (155)
22	GNOMAD	ss4259130830	Apr 27, 2021 (155)
23	GNOMAD	ss4259130831	Apr 27, 2021 (155)
24	GNOMAD	ss4259130832	Apr 27, 2021 (155)
25	GNOMAD	ss4259130833	Apr 27, 2021 (155)
26	GNOMAD	ss4259130834	Apr 27, 2021 (155)
27	GNOMAD	ss4259130835	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5208193543	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5208193544	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5208193545	Apr 27, 2021 (155)
31	1000G_HIGH_COVERAGE	ss5292255277	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5292255278	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5292255279	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5292255280	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5486856267	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5486856268	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5486856269	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5486856270	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5758526410	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5758526411	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5758526412	Oct 16, 2022 (156)
42	EVA	ss5850549258	Oct 16, 2022 (156)
43	EVA	ss5980761662	Oct 16, 2022 (156)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 419526324 (NC_000012.12:111874773::T 613/99334) Row 419526325 (NC_000012.12:111874773::TT 1/99342) Row 419526326 (NC_000012.12:111874773::TTTT 1/99344)...	-	Apr 27, 2021 (155)
53	Northern Sweden	NC_000012.11 - 112312578	Jul 13, 2019 (153)
54	8.3KJPN Submission ignored due to conflicting rows: Row 66162850 (NC_000012.11:112312577:TT: 1993/15998) Row 66162851 (NC_000012.11:112312577:T: 7881/15998) Row 66162852 (NC_000012.11:112312577::T 10/15998)	-	Apr 27, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 66162850 (NC_000012.11:112312577:TT: 1993/15998) Row 66162851 (NC_000012.11:112312577:T: 7881/15998) Row 66162852 (NC_000012.11:112312577::T 10/15998)	-	Apr 27, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 66162850 (NC_000012.11:112312577:TT: 1993/15998) Row 66162851 (NC_000012.11:112312577:T: 7881/15998) Row 66162852 (NC_000012.11:112312577::T 10/15998)	-	Apr 27, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 92363514 (NC_000012.12:111874773:T: 14255/27540) Row 92363515 (NC_000012.12:111874773:TT: 3768/27540) Row 92363516 (NC_000012.12:111874773::T 27/27540)	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 92363514 (NC_000012.12:111874773:T: 14255/27540) Row 92363515 (NC_000012.12:111874773:TT: 3768/27540) Row 92363516 (NC_000012.12:111874773::T 27/27540)	-	Oct 16, 2022 (156)
59	14KJPN Submission ignored due to conflicting rows: Row 92363514 (NC_000012.12:111874773:T: 14255/27540) Row 92363515 (NC_000012.12:111874773:TT: 3768/27540) Row 92363516 (NC_000012.12:111874773::T 27/27540)	-	Oct 16, 2022 (156)
60	ALFA	NC_000012.12 - 111874774	Apr 27, 2021 (155)

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

Associated ID	History Updated (Build)
rs35974942	May 11, 2012 (137)
rs57771519	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4259130835	NC_000012.12:111874773:TTTTTTT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4259130834	NC_000012.12:111874773:TTTTT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4259130833	NC_000012.12:111874773:TTTT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3694478218, ss4259130832, ss5292255280, ss5486856268	NC_000012.12:111874773:TTT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss294774751	NC_000012.10:110796977:TT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
12672061, ss3010358590, ss3739387196, ss3787337513, ss3792419559, ss3797302643, ss3833328931, ss5208193543, ss5980761662	NC_000012.11:112312577:TT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3064576166, ss3065497890, ss4259130831, ss5292255278, ss5486856269, ss5758526411, ss5850549258	NC_000012.12:111874773:TT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3694478219	NC_000012.12:111874774:TT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss79902288, ss80106706	NC_000012.9:110775315:T:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss294774752	NC_000012.10:110796978:T:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5208193544	NC_000012.11:112312577:T:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4259130830, ss5292255277, ss5486856267, ss5758526410	NC_000012.12:111874773:T:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3694478220	NC_000012.12:111874775:T:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss40220268	NT_009775.17:2889107:T:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss40129020	NT_009775.17:2889108:T:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5208193545	NC_000012.11:112312577::T	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4259130827, ss5292255279, ss5486856270, ss5758526412	NC_000012.12:111874773::T	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3694478221	NC_000012.12:111874776::T	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4259130828	NC_000012.12:111874773::TT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4259130829	NC_000012.12:111874773::TTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
15117642	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3181833352	NC_000012.12:111874773:TTTTTTTTT:	NC_000012.12:111874773:TTTTTTTTTTT… NC_000012.12:111874773:TTTTTTTTTTTTTTTTTTT: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 rs34005167

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

rs34005167