Name: rs34191835
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.

rs34191835

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:65016921-65016940 (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)₁₀ / del(T)₈ / del(T)₄ / del…
del(T)₁₀ / del(T)₈ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₀
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₀=0.000019 (5/264690, TOPMED)
dupT=0.06434 (701/10896, ALFA)
dupT=0.2668 (1336/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAX : Intron Variant
CHURC1-FNTB : Intron Variant
FNTB : 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	10896	TTTTTTTTTTTTTTTTTTTT=0.88822	TTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00330, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.06434, TTTTTTTTTTTTTTTTTTTTTT=0.00073, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.03910, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00330, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00101	0.902434	0.027334	0.070231	32
European	Sub	9726	TTTTTTTTTTTTTTTTTTTT=0.8750	TTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0037, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0719, TTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0438, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0037, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0011	0.889767	0.030721	0.079512	32
African	Sub	698	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	28	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	670	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	22	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	14	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	46	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	178	TTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	42	TTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	184	TTTTTTTTTTTTTTTTTTTT=0.989	TTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.011, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.98913	0.01087	0.0	32

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
TopMed	Global	Study-wide	264690	(T)₂₀=0.999981	del(T)₁₀=0.000019
Allele Frequency Aggregator	Total	Global	10896	(T)₂₀=0.88822	del(T)₁₀=0.00000, del(T)₈=0.00330, del(T)₄=0.00000, delTT=0.00000, delT=0.00000, dupT=0.06434, dupTT=0.00073, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.03910, dup(T)₆=0.00330, dup(T)₇=0.00101
Allele Frequency Aggregator	European	Sub	9726	(T)₂₀=0.8750	del(T)₁₀=0.0000, del(T)₈=0.0037, del(T)₄=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0719, dupTT=0.0008, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0438, dup(T)₆=0.0037, dup(T)₇=0.0011
Allele Frequency Aggregator	African	Sub	698	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₄=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, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	184	(T)₂₀=0.989	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₄=0.000, delTT=0.000, delT=0.000, dupT=0.011, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	178	(T)₂₀=1.000	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₄=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, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	46	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₄=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, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	42	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₄=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, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	22	(T)₂₀=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₄=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, dup(T)₇=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.2668
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.2693
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.3740
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.2008
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.281
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.182

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 14	NC_000014.9:g.65016931_65016940del
GRCh38.p14 chr 14	NC_000014.9:g.65016933_65016940del
GRCh38.p14 chr 14	NC_000014.9:g.65016937_65016940del
GRCh38.p14 chr 14	NC_000014.9:g.65016938_65016940del
GRCh38.p14 chr 14	NC_000014.9:g.65016939_65016940del
GRCh38.p14 chr 14	NC_000014.9:g.65016940del
GRCh38.p14 chr 14	NC_000014.9:g.65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016939_65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016938_65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016937_65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016936_65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016935_65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016934_65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016933_65016940dup
GRCh38.p14 chr 14	NC_000014.9:g.65016931_65016940dup
GRCh37.p13 chr 14	NC_000014.8:g.65483649_65483658del
GRCh37.p13 chr 14	NC_000014.8:g.65483651_65483658del
GRCh37.p13 chr 14	NC_000014.8:g.65483655_65483658del
GRCh37.p13 chr 14	NC_000014.8:g.65483656_65483658del
GRCh37.p13 chr 14	NC_000014.8:g.65483657_65483658del
GRCh37.p13 chr 14	NC_000014.8:g.65483658del
GRCh37.p13 chr 14	NC_000014.8:g.65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483657_65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483656_65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483655_65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483654_65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483653_65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483652_65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483651_65483658dup
GRCh37.p13 chr 14	NC_000014.8:g.65483649_65483658dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90580_90589del
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90582_90589del
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90586_90589del
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90587_90589del
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90588_90589del
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90589del
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90588_90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90587_90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90586_90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90585_90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90584_90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90583_90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90582_90589dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90580_90589dup

Gene: CHURC1-FNTB, CHURC1-FNTB readthrough (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CHURC1-FNTB transcript variant 2	NM_001202558.2:c.236+1215… NM_001202558.2:c.236+1215_236+1224del	N/A	Intron Variant
CHURC1-FNTB transcript variant 1	NM_001202559.1:c.557+1215… NM_001202559.1:c.557+1215_557+1224del	N/A	Intron Variant

Gene: MAX, MYC associated factor X (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAX transcript variant 8	NM_001271069.2:c.145-1064… NM_001271069.2:c.145-10646_145-10637del	N/A	Intron Variant
MAX transcript variant 6	NM_197957.4:c.172-10646_1… NM_197957.4:c.172-10646_172-10637del	N/A	Intron Variant
MAX transcript variant 7	NM_001271068.2:c.	N/A	Genic Downstream Transcript Variant
MAX transcript variant 11	NM_001320415.2:c.	N/A	Genic Downstream Transcript Variant
MAX transcript variant 1	NM_002382.5:c.	N/A	Genic Downstream Transcript Variant
MAX transcript variant 2	NM_145112.3:c.	N/A	Genic Downstream Transcript Variant
MAX transcript variant 3	NM_145113.3:c.	N/A	Genic Downstream Transcript Variant
MAX transcript variant 4	NM_145114.3:c.	N/A	Genic Downstream Transcript Variant
MAX transcript variant 9	NR_073137.1:n.	N/A	Genic Downstream Transcript Variant
MAX transcript variant 10	NR_073138.1:n.	N/A	Genic Downstream Transcript Variant
MAX transcript variant X1	XM_011536773.4:c.	N/A	Genic Downstream Transcript Variant
MAX transcript variant X4	XR_007064012.1:n.	N/A	Genic Downstream Transcript Variant
MAX transcript variant X2	XR_943450.4:n.	N/A	Genic Downstream Transcript Variant
MAX transcript variant X3	XR_943452.4:n.	N/A	Genic Downstream Transcript Variant

Gene: FNTB, farnesyltransferase, CAAX box, beta (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FNTB transcript	NM_002028.4:c.374+1215_37… NM_002028.4:c.374+1215_374+1224del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(T)₂₀=	del(T)₁₀	del(T)₈	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₀
GRCh38.p14 chr 14	NC_000014.9:g.65016921_65016940=	NC_000014.9:g.65016931_65016940del	NC_000014.9:g.65016933_65016940del	NC_000014.9:g.65016937_65016940del	NC_000014.9:g.65016938_65016940del	NC_000014.9:g.65016939_65016940del	NC_000014.9:g.65016940del	NC_000014.9:g.65016940dup	NC_000014.9:g.65016939_65016940dup	NC_000014.9:g.65016938_65016940dup	NC_000014.9:g.65016937_65016940dup	NC_000014.9:g.65016936_65016940dup	NC_000014.9:g.65016935_65016940dup	NC_000014.9:g.65016934_65016940dup	NC_000014.9:g.65016933_65016940dup	NC_000014.9:g.65016931_65016940dup
GRCh37.p13 chr 14	NC_000014.8:g.65483639_65483658=	NC_000014.8:g.65483649_65483658del	NC_000014.8:g.65483651_65483658del	NC_000014.8:g.65483655_65483658del	NC_000014.8:g.65483656_65483658del	NC_000014.8:g.65483657_65483658del	NC_000014.8:g.65483658del	NC_000014.8:g.65483658dup	NC_000014.8:g.65483657_65483658dup	NC_000014.8:g.65483656_65483658dup	NC_000014.8:g.65483655_65483658dup	NC_000014.8:g.65483654_65483658dup	NC_000014.8:g.65483653_65483658dup	NC_000014.8:g.65483652_65483658dup	NC_000014.8:g.65483651_65483658dup	NC_000014.8:g.65483649_65483658dup
MAX RefSeqGene (LRG_530)	NG_029830.1:g.90570_90589=	NG_029830.1:g.90580_90589del	NG_029830.1:g.90582_90589del	NG_029830.1:g.90586_90589del	NG_029830.1:g.90587_90589del	NG_029830.1:g.90588_90589del	NG_029830.1:g.90589del	NG_029830.1:g.90589dup	NG_029830.1:g.90588_90589dup	NG_029830.1:g.90587_90589dup	NG_029830.1:g.90586_90589dup	NG_029830.1:g.90585_90589dup	NG_029830.1:g.90584_90589dup	NG_029830.1:g.90583_90589dup	NG_029830.1:g.90582_90589dup	NG_029830.1:g.90580_90589dup
CHURC1-FNTB transcript variant 2	NM_001202558.1:c.236+1205=	NM_001202558.1:c.236+1215_236+1224del	NM_001202558.1:c.236+1217_236+1224del	NM_001202558.1:c.236+1221_236+1224del	NM_001202558.1:c.236+1222_236+1224del	NM_001202558.1:c.236+1223_236+1224del	NM_001202558.1:c.236+1224del	NM_001202558.1:c.236+1224dup	NM_001202558.1:c.236+1223_236+1224dup	NM_001202558.1:c.236+1222_236+1224dup	NM_001202558.1:c.236+1221_236+1224dup	NM_001202558.1:c.236+1220_236+1224dup	NM_001202558.1:c.236+1219_236+1224dup	NM_001202558.1:c.236+1218_236+1224dup	NM_001202558.1:c.236+1217_236+1224dup	NM_001202558.1:c.236+1215_236+1224dup
CHURC1-FNTB transcript variant 2	NM_001202558.2:c.236+1205=	NM_001202558.2:c.236+1215_236+1224del	NM_001202558.2:c.236+1217_236+1224del	NM_001202558.2:c.236+1221_236+1224del	NM_001202558.2:c.236+1222_236+1224del	NM_001202558.2:c.236+1223_236+1224del	NM_001202558.2:c.236+1224del	NM_001202558.2:c.236+1224dup	NM_001202558.2:c.236+1223_236+1224dup	NM_001202558.2:c.236+1222_236+1224dup	NM_001202558.2:c.236+1221_236+1224dup	NM_001202558.2:c.236+1220_236+1224dup	NM_001202558.2:c.236+1219_236+1224dup	NM_001202558.2:c.236+1218_236+1224dup	NM_001202558.2:c.236+1217_236+1224dup	NM_001202558.2:c.236+1215_236+1224dup
CHURC1-FNTB transcript variant 1	NM_001202559.1:c.557+1205=	NM_001202559.1:c.557+1215_557+1224del	NM_001202559.1:c.557+1217_557+1224del	NM_001202559.1:c.557+1221_557+1224del	NM_001202559.1:c.557+1222_557+1224del	NM_001202559.1:c.557+1223_557+1224del	NM_001202559.1:c.557+1224del	NM_001202559.1:c.557+1224dup	NM_001202559.1:c.557+1223_557+1224dup	NM_001202559.1:c.557+1222_557+1224dup	NM_001202559.1:c.557+1221_557+1224dup	NM_001202559.1:c.557+1220_557+1224dup	NM_001202559.1:c.557+1219_557+1224dup	NM_001202559.1:c.557+1218_557+1224dup	NM_001202559.1:c.557+1217_557+1224dup	NM_001202559.1:c.557+1215_557+1224dup
MAX transcript variant 8	NM_001271069.1:c.145-10637=	NM_001271069.1:c.145-10646_145-10637del	NM_001271069.1:c.145-10644_145-10637del	NM_001271069.1:c.145-10640_145-10637del	NM_001271069.1:c.145-10639_145-10637del	NM_001271069.1:c.145-10638_145-10637del	NM_001271069.1:c.145-10637del	NM_001271069.1:c.145-10637dup	NM_001271069.1:c.145-10638_145-10637dup	NM_001271069.1:c.145-10639_145-10637dup	NM_001271069.1:c.145-10640_145-10637dup	NM_001271069.1:c.145-10641_145-10637dup	NM_001271069.1:c.145-10642_145-10637dup	NM_001271069.1:c.145-10643_145-10637dup	NM_001271069.1:c.145-10644_145-10637dup	NM_001271069.1:c.145-10646_145-10637dup
MAX transcript variant 8	NM_001271069.2:c.145-10637=	NM_001271069.2:c.145-10646_145-10637del	NM_001271069.2:c.145-10644_145-10637del	NM_001271069.2:c.145-10640_145-10637del	NM_001271069.2:c.145-10639_145-10637del	NM_001271069.2:c.145-10638_145-10637del	NM_001271069.2:c.145-10637del	NM_001271069.2:c.145-10637dup	NM_001271069.2:c.145-10638_145-10637dup	NM_001271069.2:c.145-10639_145-10637dup	NM_001271069.2:c.145-10640_145-10637dup	NM_001271069.2:c.145-10641_145-10637dup	NM_001271069.2:c.145-10642_145-10637dup	NM_001271069.2:c.145-10643_145-10637dup	NM_001271069.2:c.145-10644_145-10637dup	NM_001271069.2:c.145-10646_145-10637dup
FNTB transcript	NM_002028.3:c.374+1205=	NM_002028.3:c.374+1215_374+1224del	NM_002028.3:c.374+1217_374+1224del	NM_002028.3:c.374+1221_374+1224del	NM_002028.3:c.374+1222_374+1224del	NM_002028.3:c.374+1223_374+1224del	NM_002028.3:c.374+1224del	NM_002028.3:c.374+1224dup	NM_002028.3:c.374+1223_374+1224dup	NM_002028.3:c.374+1222_374+1224dup	NM_002028.3:c.374+1221_374+1224dup	NM_002028.3:c.374+1220_374+1224dup	NM_002028.3:c.374+1219_374+1224dup	NM_002028.3:c.374+1218_374+1224dup	NM_002028.3:c.374+1217_374+1224dup	NM_002028.3:c.374+1215_374+1224dup
FNTB transcript	NM_002028.4:c.374+1205=	NM_002028.4:c.374+1215_374+1224del	NM_002028.4:c.374+1217_374+1224del	NM_002028.4:c.374+1221_374+1224del	NM_002028.4:c.374+1222_374+1224del	NM_002028.4:c.374+1223_374+1224del	NM_002028.4:c.374+1224del	NM_002028.4:c.374+1224dup	NM_002028.4:c.374+1223_374+1224dup	NM_002028.4:c.374+1222_374+1224dup	NM_002028.4:c.374+1221_374+1224dup	NM_002028.4:c.374+1220_374+1224dup	NM_002028.4:c.374+1219_374+1224dup	NM_002028.4:c.374+1218_374+1224dup	NM_002028.4:c.374+1217_374+1224dup	NM_002028.4:c.374+1215_374+1224dup
MAX transcript variant 6	NM_197957.3:c.172-10637=	NM_197957.3:c.172-10646_172-10637del	NM_197957.3:c.172-10644_172-10637del	NM_197957.3:c.172-10640_172-10637del	NM_197957.3:c.172-10639_172-10637del	NM_197957.3:c.172-10638_172-10637del	NM_197957.3:c.172-10637del	NM_197957.3:c.172-10637dup	NM_197957.3:c.172-10638_172-10637dup	NM_197957.3:c.172-10639_172-10637dup	NM_197957.3:c.172-10640_172-10637dup	NM_197957.3:c.172-10641_172-10637dup	NM_197957.3:c.172-10642_172-10637dup	NM_197957.3:c.172-10643_172-10637dup	NM_197957.3:c.172-10644_172-10637dup	NM_197957.3:c.172-10646_172-10637dup
MAX transcript variant 6	NM_197957.4:c.172-10637=	NM_197957.4:c.172-10646_172-10637del	NM_197957.4:c.172-10644_172-10637del	NM_197957.4:c.172-10640_172-10637del	NM_197957.4:c.172-10639_172-10637del	NM_197957.4:c.172-10638_172-10637del	NM_197957.4:c.172-10637del	NM_197957.4:c.172-10637dup	NM_197957.4:c.172-10638_172-10637dup	NM_197957.4:c.172-10639_172-10637dup	NM_197957.4:c.172-10640_172-10637dup	NM_197957.4:c.172-10641_172-10637dup	NM_197957.4:c.172-10642_172-10637dup	NM_197957.4:c.172-10643_172-10637dup	NM_197957.4:c.172-10644_172-10637dup	NM_197957.4:c.172-10646_172-10637dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

44 SubSNP, 29 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss40438602	Mar 13, 2006 (126)
2	PJP	ss294836117	Oct 12, 2018 (152)
3	1000GENOMES	ss1374207835	Aug 21, 2014 (142)
4	SWEGEN	ss3012351771	Nov 08, 2017 (151)
5	KHV_HUMAN_GENOMES	ss3817768488	Jul 13, 2019 (153)
6	EVA	ss3833967326	Apr 27, 2020 (154)
7	GNOMAD	ss4279660654	Apr 27, 2021 (155)
8	GNOMAD	ss4279660655	Apr 27, 2021 (155)
9	GNOMAD	ss4279660656	Apr 27, 2021 (155)
10	GNOMAD	ss4279660657	Apr 27, 2021 (155)
11	GNOMAD	ss4279660658	Apr 27, 2021 (155)
12	GNOMAD	ss4279660659	Apr 27, 2021 (155)
13	GNOMAD	ss4279660660	Apr 27, 2021 (155)
14	GNOMAD	ss4279660661	Apr 27, 2021 (155)
15	GNOMAD	ss4279660662	Apr 27, 2021 (155)
16	GNOMAD	ss4279660663	Apr 27, 2021 (155)
17	GNOMAD	ss4279660664	Apr 27, 2021 (155)
18	GNOMAD	ss4279660665	Apr 27, 2021 (155)
19	GNOMAD	ss4279660666	Apr 27, 2021 (155)
20	GNOMAD	ss4279660667	Apr 27, 2021 (155)
21	GNOMAD	ss4279660668	Apr 27, 2021 (155)
22	TOPMED	ss4973884499	Apr 27, 2021 (155)
23	TOMMO_GENOMICS	ss5213653550	Apr 27, 2021 (155)
24	TOMMO_GENOMICS	ss5213653551	Apr 27, 2021 (155)
25	TOMMO_GENOMICS	ss5213653552	Apr 27, 2021 (155)
26	TOMMO_GENOMICS	ss5213653553	Apr 27, 2021 (155)
27	TOMMO_GENOMICS	ss5213653554	Apr 27, 2021 (155)
28	1000G_HIGH_COVERAGE	ss5296549705	Oct 16, 2022 (156)
29	1000G_HIGH_COVERAGE	ss5296549706	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5296549707	Oct 16, 2022 (156)
31	HUGCELL_USP	ss5490560480	Oct 16, 2022 (156)
32	HUGCELL_USP	ss5490560481	Oct 16, 2022 (156)
33	HUGCELL_USP	ss5490560482	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5490560483	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5490560484	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5490560485	Oct 16, 2022 (156)
37	TOMMO_GENOMICS	ss5766577825	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5766577826	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5766577827	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5766577828	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5766577829	Oct 16, 2022 (156)
42	TOMMO_GENOMICS	ss5766577830	Oct 16, 2022 (156)
43	EVA	ss5851073196	Oct 16, 2022 (156)
44	EVA	ss5901715078	Oct 16, 2022 (156)
45	1000Genomes	NC_000014.8 - 65483639	Oct 12, 2018 (152)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 453881967 (NC_000014.9:65016920::T 32700/106374) Row 453881968 (NC_000014.9:65016920::TT 1092/106538) Row 453881969 (NC_000014.9:65016920::TTT 44/106556)...	-	Apr 27, 2021 (155)
61	8.3KJPN Submission ignored due to conflicting rows: Row 71622857 (NC_000014.8:65483638:T: 707/16512) Row 71622858 (NC_000014.8:65483638::T 7187/16512) Row 71622859 (NC_000014.8:65483638::TT 79/16512)...	-	Apr 27, 2021 (155)
62	8.3KJPN Submission ignored due to conflicting rows: Row 71622857 (NC_000014.8:65483638:T: 707/16512) Row 71622858 (NC_000014.8:65483638::T 7187/16512) Row 71622859 (NC_000014.8:65483638::TT 79/16512)...	-	Apr 27, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 71622857 (NC_000014.8:65483638:T: 707/16512) Row 71622858 (NC_000014.8:65483638::T 7187/16512) Row 71622859 (NC_000014.8:65483638::TT 79/16512)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 71622857 (NC_000014.8:65483638:T: 707/16512) Row 71622858 (NC_000014.8:65483638::T 7187/16512) Row 71622859 (NC_000014.8:65483638::TT 79/16512)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 71622857 (NC_000014.8:65483638:T: 707/16512) Row 71622858 (NC_000014.8:65483638::T 7187/16512) Row 71622859 (NC_000014.8:65483638::TT 79/16512)...	-	Apr 27, 2021 (155)
66	14KJPN Submission ignored due to conflicting rows: Row 100414929 (NC_000014.9:65016920::T 13769/28246) Row 100414930 (NC_000014.9:65016920:T: 1429/28246) Row 100414931 (NC_000014.9:65016920::TT 147/28246)...	-	Oct 16, 2022 (156)
67	14KJPN Submission ignored due to conflicting rows: Row 100414929 (NC_000014.9:65016920::T 13769/28246) Row 100414930 (NC_000014.9:65016920:T: 1429/28246) Row 100414931 (NC_000014.9:65016920::TT 147/28246)...	-	Oct 16, 2022 (156)
68	14KJPN Submission ignored due to conflicting rows: Row 100414929 (NC_000014.9:65016920::T 13769/28246) Row 100414930 (NC_000014.9:65016920:T: 1429/28246) Row 100414931 (NC_000014.9:65016920::TT 147/28246)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 100414929 (NC_000014.9:65016920::T 13769/28246) Row 100414930 (NC_000014.9:65016920:T: 1429/28246) Row 100414931 (NC_000014.9:65016920::TT 147/28246)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 100414929 (NC_000014.9:65016920::T 13769/28246) Row 100414930 (NC_000014.9:65016920:T: 1429/28246) Row 100414931 (NC_000014.9:65016920::TT 147/28246)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 100414929 (NC_000014.9:65016920::T 13769/28246) Row 100414930 (NC_000014.9:65016920:T: 1429/28246) Row 100414931 (NC_000014.9:65016920::TT 147/28246)...	-	Oct 16, 2022 (156)
72	TopMed	NC_000014.9 - 65016921	Apr 27, 2021 (155)
73	ALFA	NC_000014.9 - 65016921	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
189430158, ss4279660668, ss4973884499	NC_000014.9:65016920:TTTTTTTTTT:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss3012351771	NC_000014.8:65483638:TTTTTTTT:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4279660667, ss5490560483, ss5901715078	NC_000014.9:65016920:TTTTTTTT:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4279660666	NC_000014.9:65016920:TTTT:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4279660665	NC_000014.9:65016920:TTT:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5213653554	NC_000014.8:65483638:TT:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4279660664, ss5766577829	NC_000014.9:65016920:TT:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss5213653550	NC_000014.8:65483638:T:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4279660663, ss5490560484, ss5766577826	NC_000014.9:65016920:T:	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss294836117	NC_000014.7:64553411::T	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
64371294, ss1374207835, ss3833967326, ss5213653551	NC_000014.8:65483638::T	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3817768488, ss4279660654, ss5296549705, ss5490560480, ss5766577825, ss5851073196	NC_000014.9:65016920::T	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss40438602	NT_026437.12:46483638::T	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5213653552	NC_000014.8:65483638::TT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660655, ss5296549707, ss5490560481, ss5766577827	NC_000014.9:65016920::TT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660656, ss5766577830	NC_000014.9:65016920::TTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660657	NC_000014.9:65016920::TTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5213653553	NC_000014.8:65483638::TTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660658, ss5296549706, ss5490560482, ss5766577828	NC_000014.9:65016920::TTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660659, ss5490560485	NC_000014.9:65016920::TTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660660	NC_000014.9:65016920::TTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
107071859	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660661	NC_000014.9:65016920::TTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4279660662	NC_000014.9:65016920::TTTTTTTTTT	NC_000014.9:65016920:TTTTTTTTTTTTT… NC_000014.9:65016920:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs34191835

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

rs34191835