Name: rs34115919
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.

rs34115919

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr5:60944706-60944715 (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: delCCC / delCC / delC / dupC / dup…
delCCC / delCC / delC / dupC / dupCC / dupCCC / dup(C)₄ / dup(C)₅ / dup(C)₆
Variation Type: Indel Insertion and Deletion
Frequency: delC=0.1976 (1344/6802, ALFA)
(C)₁₀=0.3768 (1887/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ERCC8 : Intron Variant
NDUFAF2 : 2KB Upstream 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	6802	CCCCCCCCCC=0.6558	CCCCCCC=0.0000, CCCCCCCC=0.0897, CCCCCCCCC=0.1976, CCCCCCCCCCC=0.0565, CCCCCCCCCCCC=0.0004, CCCCCCCCCCCCC=0.0000	0.677557	0.090626	0.231816	32
European	Sub	5910	CCCCCCCCCC=0.6046	CCCCCCC=0.0000, CCCCCCCC=0.1030, CCCCCCCCC=0.2269, CCCCCCCCCCC=0.0650, CCCCCCCCCCCC=0.0005, CCCCCCCCCCCCC=0.0000	0.610536	0.109125	0.280339	32
African	Sub	708	CCCCCCCCCC=1.000	CCCCCCC=0.000, CCCCCCCC=0.000, CCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
African Others	Sub	26	CCCCCCCCCC=1.00	CCCCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
African American	Sub	682	CCCCCCCCCC=1.000	CCCCCCC=0.000, CCCCCCCC=0.000, CCCCCCCCC=0.000, CCCCCCCCCCC=0.000, CCCCCCCCCCCC=0.000, CCCCCCCCCCCCC=0.000	1.0	0.0	0.0	N/A
Asian	Sub	0	CCCCCCCCCC=0	CCCCCCC=0, CCCCCCCC=0, CCCCCCCCC=0, CCCCCCCCCCC=0, CCCCCCCCCCCC=0, CCCCCCCCCCCCC=0	0	0	0	N/A
East Asian	Sub	0	CCCCCCCCCC=0	CCCCCCC=0, CCCCCCCC=0, CCCCCCCCC=0, CCCCCCCCCCC=0, CCCCCCCCCCCC=0, CCCCCCCCCCCCC=0	0	0	0	N/A
Other Asian	Sub	0	CCCCCCCCCC=0	CCCCCCC=0, CCCCCCCC=0, CCCCCCCCC=0, CCCCCCCCCCC=0, CCCCCCCCCCCC=0, CCCCCCCCCCCCC=0	0	0	0	N/A
Latin American 1	Sub	20	CCCCCCCCCC=1.00	CCCCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	56	CCCCCCCCCC=1.00	CCCCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	18	CCCCCCCCCC=1.00	CCCCCCC=0.00, CCCCCCCC=0.00, CCCCCCCCC=0.00, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00	1.0	0.0	0.0	N/A
Other	Sub	90	CCCCCCCCCC=0.96	CCCCCCC=0.00, CCCCCCCC=0.01, CCCCCCCCC=0.03, CCCCCCCCCCC=0.00, CCCCCCCCCCCC=0.00, CCCCCCCCCCCCC=0.00	0.977273	0.022727	0.0	24

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	6802	(C)₁₀=0.6558	delCCC=0.0000, delCC=0.0897, delC=0.1976, dupC=0.0565, dupCC=0.0004, dupCCC=0.0000
Allele Frequency Aggregator	European	Sub	5910	(C)₁₀=0.6046	delCCC=0.0000, delCC=0.1030, delC=0.2269, dupC=0.0650, dupCC=0.0005, dupCCC=0.0000
Allele Frequency Aggregator	African	Sub	708	(C)₁₀=1.000	delCCC=0.000, delCC=0.000, delC=0.000, dupC=0.000, dupCC=0.000, dupCCC=0.000
Allele Frequency Aggregator	Other	Sub	90	(C)₁₀=0.96	delCCC=0.00, delCC=0.01, delC=0.03, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Latin American 2	Sub	56	(C)₁₀=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Latin American 1	Sub	20	(C)₁₀=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	South Asian	Sub	18	(C)₁₀=1.00	delCCC=0.00, delCC=0.00, delC=0.00, dupC=0.00, dupCC=0.00, dupCCC=0.00
Allele Frequency Aggregator	Asian	Sub	0	(C)₁₀=0	delCCC=0, delCC=0, delC=0, dupC=0, dupCC=0, dupCCC=0
1000Genomes	Global	Study-wide	5008	(C)₁₀=0.3768	delC=0.6232
1000Genomes	African	Sub	1322	(C)₁₀=0.5552	delC=0.4448
1000Genomes	East Asian	Sub	1008	(C)₁₀=0.0754	delC=0.9246
1000Genomes	Europe	Sub	1006	(C)₁₀=0.4344	delC=0.5656
1000Genomes	South Asian	Sub	978	(C)₁₀=0.422	delC=0.578
1000Genomes	American	Sub	694	(C)₁₀=0.327	delC=0.673

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 5	NC_000005.10:g.60944713_60944715del
GRCh38.p14 chr 5	NC_000005.10:g.60944714_60944715del
GRCh38.p14 chr 5	NC_000005.10:g.60944715del
GRCh38.p14 chr 5	NC_000005.10:g.60944715dup
GRCh38.p14 chr 5	NC_000005.10:g.60944714_60944715dup
GRCh38.p14 chr 5	NC_000005.10:g.60944713_60944715dup
GRCh38.p14 chr 5	NC_000005.10:g.60944712_60944715dup
GRCh38.p14 chr 5	NC_000005.10:g.60944711_60944715dup
GRCh38.p14 chr 5	NC_000005.10:g.60944710_60944715dup
GRCh37.p13 chr 5	NC_000005.9:g.60240540_60240542del
GRCh37.p13 chr 5	NC_000005.9:g.60240541_60240542del
GRCh37.p13 chr 5	NC_000005.9:g.60240542del
GRCh37.p13 chr 5	NC_000005.9:g.60240542dup
GRCh37.p13 chr 5	NC_000005.9:g.60240541_60240542dup
GRCh37.p13 chr 5	NC_000005.9:g.60240540_60240542dup
GRCh37.p13 chr 5	NC_000005.9:g.60240539_60240542dup
GRCh37.p13 chr 5	NC_000005.9:g.60240538_60240542dup
GRCh37.p13 chr 5	NC_000005.9:g.60240537_60240542dup
NDUFAF2 RefSeqGene	NG_008978.1:g.4585_4587del
NDUFAF2 RefSeqGene	NG_008978.1:g.4586_4587del
NDUFAF2 RefSeqGene	NG_008978.1:g.4587del
NDUFAF2 RefSeqGene	NG_008978.1:g.4587dup
NDUFAF2 RefSeqGene	NG_008978.1:g.4586_4587dup
NDUFAF2 RefSeqGene	NG_008978.1:g.4585_4587dup
NDUFAF2 RefSeqGene	NG_008978.1:g.4584_4587dup
NDUFAF2 RefSeqGene	NG_008978.1:g.4583_4587dup
NDUFAF2 RefSeqGene	NG_008978.1:g.4582_4587dup
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5371_5373del
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5372_5373del
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5373del
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5373dup
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5372_5373dup
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5371_5373dup
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5370_5373dup
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5369_5373dup
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5368_5373dup

Gene: ERCC8, ERCC excision repair 8, CSA ubiquitin ligase complex subunit (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ERCC8 transcript variant 1	NM_000082.4:c.77+224_77+2… NM_000082.4:c.77+224_77+226del	N/A	Intron Variant
ERCC8 transcript variant 2	NM_001007233.3:c.-316+224… NM_001007233.3:c.-316+224_-316+226del	N/A	Intron Variant
ERCC8 transcript variant 3	NM_001007234.3:c.77+224_7… NM_001007234.3:c.77+224_77+226del	N/A	Intron Variant
ERCC8 transcript variant 4	NM_001290285.2:c.-301+224… NM_001290285.2:c.-301+224_-301+226del	N/A	Intron Variant

Gene: NDUFAF2, NADH:ubiquinone oxidoreductase complex assembly factor 2 (plus strand) : 2KB Upstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
NDUFAF2 transcript	NM_174889.5:c.	N/A	Upstream Transcript Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(C)₁₀=	delCCC	delCC	delC	dupC	dupCC	dupCCC	dup(C)₄	dup(C)₅	dup(C)₆
GRCh38.p14 chr 5	NC_000005.10:g.60944706_60944715=	NC_000005.10:g.60944713_60944715del	NC_000005.10:g.60944714_60944715del	NC_000005.10:g.60944715del	NC_000005.10:g.60944715dup	NC_000005.10:g.60944714_60944715dup	NC_000005.10:g.60944713_60944715dup	NC_000005.10:g.60944712_60944715dup	NC_000005.10:g.60944711_60944715dup	NC_000005.10:g.60944710_60944715dup
GRCh37.p13 chr 5	NC_000005.9:g.60240533_60240542=	NC_000005.9:g.60240540_60240542del	NC_000005.9:g.60240541_60240542del	NC_000005.9:g.60240542del	NC_000005.9:g.60240542dup	NC_000005.9:g.60240541_60240542dup	NC_000005.9:g.60240540_60240542dup	NC_000005.9:g.60240539_60240542dup	NC_000005.9:g.60240538_60240542dup	NC_000005.9:g.60240537_60240542dup
NDUFAF2 RefSeqGene	NG_008978.1:g.4578_4587=	NG_008978.1:g.4585_4587del	NG_008978.1:g.4586_4587del	NG_008978.1:g.4587del	NG_008978.1:g.4587dup	NG_008978.1:g.4586_4587dup	NG_008978.1:g.4585_4587dup	NG_008978.1:g.4584_4587dup	NG_008978.1:g.4583_4587dup	NG_008978.1:g.4582_4587dup
ERCC8 RefSeqGene (LRG_466)	NG_009289.1:g.5364_5373=	NG_009289.1:g.5371_5373del	NG_009289.1:g.5372_5373del	NG_009289.1:g.5373del	NG_009289.1:g.5373dup	NG_009289.1:g.5372_5373dup	NG_009289.1:g.5371_5373dup	NG_009289.1:g.5370_5373dup	NG_009289.1:g.5369_5373dup	NG_009289.1:g.5368_5373dup
ERCC8 transcript variant 1	NM_000082.3:c.77+226=	NM_000082.3:c.77+224_77+226del	NM_000082.3:c.77+225_77+226del	NM_000082.3:c.77+226del	NM_000082.3:c.77+226dup	NM_000082.3:c.77+225_77+226dup	NM_000082.3:c.77+224_77+226dup	NM_000082.3:c.77+223_77+226dup	NM_000082.3:c.77+222_77+226dup	NM_000082.3:c.77+221_77+226dup
ERCC8 transcript variant 1	NM_000082.4:c.77+226=	NM_000082.4:c.77+224_77+226del	NM_000082.4:c.77+225_77+226del	NM_000082.4:c.77+226del	NM_000082.4:c.77+226dup	NM_000082.4:c.77+225_77+226dup	NM_000082.4:c.77+224_77+226dup	NM_000082.4:c.77+223_77+226dup	NM_000082.4:c.77+222_77+226dup	NM_000082.4:c.77+221_77+226dup
ERCC8 transcript variant 2	NM_001007233.3:c.-316+226=	NM_001007233.3:c.-316+224_-316+226del	NM_001007233.3:c.-316+225_-316+226del	NM_001007233.3:c.-316+226del	NM_001007233.3:c.-316+226dup	NM_001007233.3:c.-316+225_-316+226dup	NM_001007233.3:c.-316+224_-316+226dup	NM_001007233.3:c.-316+223_-316+226dup	NM_001007233.3:c.-316+222_-316+226dup	NM_001007233.3:c.-316+221_-316+226dup
ERCC8 transcript variant 3	NM_001007234.3:c.77+226=	NM_001007234.3:c.77+224_77+226del	NM_001007234.3:c.77+225_77+226del	NM_001007234.3:c.77+226del	NM_001007234.3:c.77+226dup	NM_001007234.3:c.77+225_77+226dup	NM_001007234.3:c.77+224_77+226dup	NM_001007234.3:c.77+223_77+226dup	NM_001007234.3:c.77+222_77+226dup	NM_001007234.3:c.77+221_77+226dup
ERCC8 transcript variant 4	NM_001290285.2:c.-301+226=	NM_001290285.2:c.-301+224_-301+226del	NM_001290285.2:c.-301+225_-301+226del	NM_001290285.2:c.-301+226del	NM_001290285.2:c.-301+226dup	NM_001290285.2:c.-301+225_-301+226dup	NM_001290285.2:c.-301+224_-301+226dup	NM_001290285.2:c.-301+223_-301+226dup	NM_001290285.2:c.-301+222_-301+226dup	NM_001290285.2:c.-301+221_-301+226dup
ERCC8 transcript variant X1	XM_005248423.1:c.77+226=	XM_005248423.1:c.77+224_77+226del	XM_005248423.1:c.77+225_77+226del	XM_005248423.1:c.77+226del	XM_005248423.1:c.77+226dup	XM_005248423.1:c.77+225_77+226dup	XM_005248423.1:c.77+224_77+226dup	XM_005248423.1:c.77+223_77+226dup	XM_005248423.1:c.77+222_77+226dup	XM_005248423.1:c.77+221_77+226dup
ERCC8 transcript variant X2	XM_005248424.1:c.-301+226=	XM_005248424.1:c.-301+224_-301+226del	XM_005248424.1:c.-301+225_-301+226del	XM_005248424.1:c.-301+226del	XM_005248424.1:c.-301+226dup	XM_005248424.1:c.-301+225_-301+226dup	XM_005248424.1:c.-301+224_-301+226dup	XM_005248424.1:c.-301+223_-301+226dup	XM_005248424.1:c.-301+222_-301+226dup	XM_005248424.1:c.-301+221_-301+226dup

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#.

38 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	BUSHMAN	ss193802233	Jul 04, 2010 (132)
2	BILGI_BIOE	ss666311782	Apr 25, 2013 (138)
3	SSIP	ss947143629	Aug 21, 2014 (142)
4	1000GENOMES	ss1373862099	Aug 21, 2014 (142)
5	SYSTEMSBIOZJU	ss2626016534	Nov 08, 2017 (151)
6	MCHAISSO	ss3065031527	Nov 08, 2017 (151)
7	URBANLAB	ss3648070441	Oct 12, 2018 (152)
8	EVA_DECODE	ss3714766931	Jul 13, 2019 (153)
9	EVA_DECODE	ss3714766932	Jul 13, 2019 (153)
10	EVA_DECODE	ss3714766933	Jul 13, 2019 (153)
11	EVA_DECODE	ss3714766934	Jul 13, 2019 (153)
12	EVA_DECODE	ss3714766935	Jul 13, 2019 (153)
13	EVA_DECODE	ss3714766936	Jul 13, 2019 (153)
14	INMEGENXS	ss3745674933	Jul 13, 2019 (153)
15	PACBIO	ss3785121698	Jul 13, 2019 (153)
16	PACBIO	ss3790526504	Jul 13, 2019 (153)
17	PACBIO	ss3795403149	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3806651576	Jul 13, 2019 (153)
19	EVA	ss3829265960	Apr 26, 2020 (154)
20	KOGIC	ss3956766500	Apr 26, 2020 (154)
21	KOGIC	ss3956766501	Apr 26, 2020 (154)
22	KOGIC	ss3956766502	Apr 26, 2020 (154)
23	GNOMAD	ss4105195755	Apr 26, 2021 (155)
24	GNOMAD	ss4105195756	Apr 26, 2021 (155)
25	GNOMAD	ss4105195757	Apr 26, 2021 (155)
26	GNOMAD	ss4105195758	Apr 26, 2021 (155)
27	GNOMAD	ss4105195759	Apr 26, 2021 (155)
28	GNOMAD	ss4105195760	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5171928604	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5171928605	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5171928606	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5171928607	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5708378190	Oct 13, 2022 (156)
34	TOMMO_GENOMICS	ss5708378191	Oct 13, 2022 (156)
35	TOMMO_GENOMICS	ss5708378192	Oct 13, 2022 (156)
36	TOMMO_GENOMICS	ss5708378193	Oct 13, 2022 (156)
37	EVA	ss5834984532	Oct 13, 2022 (156)
38	EVA	ss5834984533	Oct 13, 2022 (156)
39	1000Genomes	NC_000005.9 - 60240533	Oct 12, 2018 (152)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189880529 (NC_000005.10:60944705::C 7990/89192) Row 189880530 (NC_000005.10:60944705::CC 150/89218) Row 189880531 (NC_000005.10:60944705::CCC 16/89204)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189880529 (NC_000005.10:60944705::C 7990/89192) Row 189880530 (NC_000005.10:60944705::CC 150/89218) Row 189880531 (NC_000005.10:60944705::CCC 16/89204)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189880529 (NC_000005.10:60944705::C 7990/89192) Row 189880530 (NC_000005.10:60944705::CC 150/89218) Row 189880531 (NC_000005.10:60944705::CCC 16/89204)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189880529 (NC_000005.10:60944705::C 7990/89192) Row 189880530 (NC_000005.10:60944705::CC 150/89218) Row 189880531 (NC_000005.10:60944705::CCC 16/89204)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189880529 (NC_000005.10:60944705::C 7990/89192) Row 189880530 (NC_000005.10:60944705::CC 150/89218) Row 189880531 (NC_000005.10:60944705::CCC 16/89204)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 189880529 (NC_000005.10:60944705::C 7990/89192) Row 189880530 (NC_000005.10:60944705::CC 150/89218) Row 189880531 (NC_000005.10:60944705::CCC 16/89204)...	-	Apr 26, 2021 (155)
46	Korean Genome Project Submission ignored due to conflicting rows: Row 13144501 (NC_000005.10:60944705:CC: 199/1732) Row 13144502 (NC_000005.10:60944707::C 83/1732) Row 13144503 (NC_000005.10:60944706:C: 1083/1732)	-	Apr 26, 2020 (154)
47	Korean Genome Project Submission ignored due to conflicting rows: Row 13144501 (NC_000005.10:60944705:CC: 199/1732) Row 13144502 (NC_000005.10:60944707::C 83/1732) Row 13144503 (NC_000005.10:60944706:C: 1083/1732)	-	Apr 26, 2020 (154)
48	Korean Genome Project Submission ignored due to conflicting rows: Row 13144501 (NC_000005.10:60944705:CC: 199/1732) Row 13144502 (NC_000005.10:60944707::C 83/1732) Row 13144503 (NC_000005.10:60944706:C: 1083/1732)	-	Apr 26, 2020 (154)
49	8.3KJPN Submission ignored due to conflicting rows: Row 29897911 (NC_000005.9:60240532:C: 8121/15742) Row 29897912 (NC_000005.9:60240532:CC: 1838/15742) Row 29897913 (NC_000005.9:60240532::C 671/15742)...	-	Apr 26, 2021 (155)
50	8.3KJPN Submission ignored due to conflicting rows: Row 29897911 (NC_000005.9:60240532:C: 8121/15742) Row 29897912 (NC_000005.9:60240532:CC: 1838/15742) Row 29897913 (NC_000005.9:60240532::C 671/15742)...	-	Apr 26, 2021 (155)
51	8.3KJPN Submission ignored due to conflicting rows: Row 29897911 (NC_000005.9:60240532:C: 8121/15742) Row 29897912 (NC_000005.9:60240532:CC: 1838/15742) Row 29897913 (NC_000005.9:60240532::C 671/15742)...	-	Apr 26, 2021 (155)
52	8.3KJPN Submission ignored due to conflicting rows: Row 29897911 (NC_000005.9:60240532:C: 8121/15742) Row 29897912 (NC_000005.9:60240532:CC: 1838/15742) Row 29897913 (NC_000005.9:60240532::C 671/15742)...	-	Apr 26, 2021 (155)
53	14KJPN Submission ignored due to conflicting rows: Row 42215294 (NC_000005.10:60944705:C: 16132/27986) Row 42215295 (NC_000005.10:60944705:CC: 3617/27986) Row 42215296 (NC_000005.10:60944705::C 1434/27986)...	-	Oct 13, 2022 (156)
54	14KJPN Submission ignored due to conflicting rows: Row 42215294 (NC_000005.10:60944705:C: 16132/27986) Row 42215295 (NC_000005.10:60944705:CC: 3617/27986) Row 42215296 (NC_000005.10:60944705::C 1434/27986)...	-	Oct 13, 2022 (156)
55	14KJPN Submission ignored due to conflicting rows: Row 42215294 (NC_000005.10:60944705:C: 16132/27986) Row 42215295 (NC_000005.10:60944705:CC: 3617/27986) Row 42215296 (NC_000005.10:60944705::C 1434/27986)...	-	Oct 13, 2022 (156)
56	14KJPN Submission ignored due to conflicting rows: Row 42215294 (NC_000005.10:60944705:C: 16132/27986) Row 42215295 (NC_000005.10:60944705:CC: 3617/27986) Row 42215296 (NC_000005.10:60944705::C 1434/27986)...	-	Oct 13, 2022 (156)
57	ALFA	NC_000005.10 - 60944706	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
8163536399	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCC	(self)
ss947143629, ss3745674933, ss5171928605, ss5834984533	NC_000005.9:60240532:CC:	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCC	(self)
ss3065031527, ss3648070441, ss3714766936, ss3956766500, ss5708378191	NC_000005.10:60944705:CC:	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCC	(self)
8163536399	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCC	(self)
ss193802233	NT_034772.7:10834898:CC:	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCC	(self)
26871775, ss666311782, ss1373862099, ss2626016534, ss3785121698, ss3790526504, ss3795403149, ss3829265960, ss5171928604, ss5834984532	NC_000005.9:60240532:C:	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCC	(self)
ss3806651576, ss5708378190	NC_000005.10:60944705:C:	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCC	(self)
8163536399	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCC	(self)
ss3714766935, ss3956766502	NC_000005.10:60944706:C:	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCC	(self)
ss5171928606	NC_000005.9:60240532::C	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCC	(self)
ss4105195755, ss5708378192	NC_000005.10:60944705::C	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCC	(self)
8163536399	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCC	(self)
ss3714766934, ss3956766501	NC_000005.10:60944707::C	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCC	(self)
ss5171928607	NC_000005.9:60240532::CC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCC	(self)
ss4105195756, ss5708378193	NC_000005.10:60944705::CC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCC	(self)
8163536399	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCC	(self)
ss3714766933	NC_000005.10:60944707::CC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCC	(self)
ss4105195757	NC_000005.10:60944705::CCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCC	(self)
8163536399	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss3714766932	NC_000005.10:60944707::CCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCC	(self)
ss4105195758	NC_000005.10:60944705::CCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCCC	(self)
ss4105195759	NC_000005.10:60944705::CCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
ss3714766931	NC_000005.10:60944707::CCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCCCC	(self)
ss4105195760	NC_000005.10:60944705::CCCCCC	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCCCCCCCCCCC	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3465574974	NC_000005.10:60944705:CCC:	NC_000005.10:60944705:CCCCCCCCCC:C… NC_000005.10:60944705:CCCCCCCCCC:CCCCCCC

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

No publications for rs34115919

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

rs34115919