Name: rs35399198
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.

rs35399198

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:99973081-99973112 (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(ATTT)₄ / del(ATTT)₃ / del(ATTT…
del(ATTT)₄ / del(ATTT)₃ / del(ATTT)₂ / delATTT / dupATTT / dup(ATTT)₂ / dup(ATTT)₃ / dup(ATTT)₄ / dup(ATTT)₅ / dup(ATTT)₆ / dup(ATTT)₇ / dup(ATTT)₈ / ins(ATTT)₉
Variation Type: Indel Insertion and Deletion
Frequency: dup(ATTT)₄=0.000321 (85/264690, TOPMED)
(ATTT)₈=0.3978 (1992/5008, 1000G)
dupATTT=0.3296 (1627/4936, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DNMBP : 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	4936	ATTTATTTATTTATTTATTTATTTATTTATTT=0.2089	ATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTTATTT=0.3722, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.3296, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0841, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0045, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0008, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0000	0.281157	0.23368	0.485163	1
European	Sub	4674	ATTTATTTATTTATTTATTTATTTATTTATTT=0.1660	ATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTTATTT=0.3922, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.3477, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0886, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0047, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0009, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0000	0.281575	0.234027	0.484398	1
African	Sub	176	ATTTATTTATTTATTTATTTATTTATTTATTT=1.000	ATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000	0	0	0	N/A
African Others	Sub	4	ATTTATTTATTTATTTATTTATTTATTTATTT=1.0	ATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0	0	0	0	N/A
African American	Sub	172	ATTTATTTATTTATTTATTTATTTATTTATTT=1.000	ATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.000	0	0	0	N/A
Asian	Sub	22	ATTTATTTATTTATTTATTTATTTATTTATTT=1.00	ATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00	0	0	0	N/A
East Asian	Sub	18	ATTTATTTATTTATTTATTTATTTATTTATTT=1.00	ATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00	0	0	0	N/A
Other Asian	Sub	4	ATTTATTTATTTATTTATTTATTTATTTATTT=1.0	ATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0	0	0	0	N/A
Latin American 1	Sub	10	ATTTATTTATTTATTTATTTATTTATTTATTT=1.0	ATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0	0	0	0	N/A
Latin American 2	Sub	12	ATTTATTTATTTATTTATTTATTTATTTATTT=1.00	ATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00	0	0	0	N/A
South Asian	Sub	4	ATTTATTTATTTATTTATTTATTTATTTATTT=1.0	ATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.0	0	0	0	N/A
Other	Sub	38	ATTTATTTATTTATTTATTTATTTATTTATTT=0.82	ATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTT=0.11, ATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.05, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.03, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00, ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT=0.00	0.0	0.0	1.0	1

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	- No frequency provided	dup(ATTT)₄=0.000321
1000Genomes	Global	Study-wide	5008	(ATTT)₈=0.3978	delATTT=0.6022
1000Genomes	African	Sub	1322	(ATTT)₈=0.3260	delATTT=0.6740
1000Genomes	East Asian	Sub	1008	(ATTT)₈=0.5992	delATTT=0.4008
1000Genomes	Europe	Sub	1006	(ATTT)₈=0.2883	delATTT=0.7117
1000Genomes	South Asian	Sub	978	(ATTT)₈=0.463	delATTT=0.537
1000Genomes	American	Sub	694	(ATTT)₈=0.308	delATTT=0.692
Allele Frequency Aggregator	Total	Global	4936	(ATTT)₈=0.2089	del(ATTT)₄=0.0000, del(ATTT)₃=0.0000, del(ATTT)₂=0.0000, delATTT=0.3722, dupATTT=0.3296, dup(ATTT)₂=0.0841, dup(ATTT)₃=0.0045, dup(ATTT)₄=0.0008, dup(ATTT)₅=0.0000, dup(ATTT)₆=0.0000, dup(ATTT)₇=0.0000
Allele Frequency Aggregator	European	Sub	4674	(ATTT)₈=0.1660	del(ATTT)₄=0.0000, del(ATTT)₃=0.0000, del(ATTT)₂=0.0000, delATTT=0.3922, dupATTT=0.3477, dup(ATTT)₂=0.0886, dup(ATTT)₃=0.0047, dup(ATTT)₄=0.0009, dup(ATTT)₅=0.0000, dup(ATTT)₆=0.0000, dup(ATTT)₇=0.0000
Allele Frequency Aggregator	African	Sub	176	(ATTT)₈=1.000	del(ATTT)₄=0.000, del(ATTT)₃=0.000, del(ATTT)₂=0.000, delATTT=0.000, dupATTT=0.000, dup(ATTT)₂=0.000, dup(ATTT)₃=0.000, dup(ATTT)₄=0.000, dup(ATTT)₅=0.000, dup(ATTT)₆=0.000, dup(ATTT)₇=0.000
Allele Frequency Aggregator	Other	Sub	38	(ATTT)₈=0.82	del(ATTT)₄=0.00, del(ATTT)₃=0.00, del(ATTT)₂=0.00, delATTT=0.11, dupATTT=0.05, dup(ATTT)₂=0.03, dup(ATTT)₃=0.00, dup(ATTT)₄=0.00, dup(ATTT)₅=0.00, dup(ATTT)₆=0.00, dup(ATTT)₇=0.00
Allele Frequency Aggregator	Asian	Sub	22	(ATTT)₈=1.00	del(ATTT)₄=0.00, del(ATTT)₃=0.00, del(ATTT)₂=0.00, delATTT=0.00, dupATTT=0.00, dup(ATTT)₂=0.00, dup(ATTT)₃=0.00, dup(ATTT)₄=0.00, dup(ATTT)₅=0.00, dup(ATTT)₆=0.00, dup(ATTT)₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	12	(ATTT)₈=1.00	del(ATTT)₄=0.00, del(ATTT)₃=0.00, del(ATTT)₂=0.00, delATTT=0.00, dupATTT=0.00, dup(ATTT)₂=0.00, dup(ATTT)₃=0.00, dup(ATTT)₄=0.00, dup(ATTT)₅=0.00, dup(ATTT)₆=0.00, dup(ATTT)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	10	(ATTT)₈=1.0	del(ATTT)₄=0.0, del(ATTT)₃=0.0, del(ATTT)₂=0.0, delATTT=0.0, dupATTT=0.0, dup(ATTT)₂=0.0, dup(ATTT)₃=0.0, dup(ATTT)₄=0.0, dup(ATTT)₅=0.0, dup(ATTT)₆=0.0, dup(ATTT)₇=0.0
Allele Frequency Aggregator	South Asian	Sub	4	(ATTT)₈=1.0	del(ATTT)₄=0.0, del(ATTT)₃=0.0, del(ATTT)₂=0.0, delATTT=0.0, dupATTT=0.0, dup(ATTT)₂=0.0, dup(ATTT)₃=0.0, dup(ATTT)₄=0.0, dup(ATTT)₅=0.0, dup(ATTT)₆=0.0, dup(ATTT)₇=0.0

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[4]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[5]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[6]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[7]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[9]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[10]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[11]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[12]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[13]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[14]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[15]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[16]
GRCh38.p14 chr 10	NC_000010.11:g.99973081ATTT[17]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[4]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[5]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[6]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[7]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[9]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[10]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[11]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[12]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[13]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[14]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[15]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[16]
GRCh37.p13 chr 10	NC_000010.10:g.101732838ATTT[17]

Gene: DNMBP, dynamin binding protein (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DNMBP transcript variant 1	NM_015221.4:c.-10-978AAAT… NM_015221.4:c.-10-978AAAT[4]	N/A	Intron Variant
DNMBP transcript variant 2	NM_001318326.2:c.	N/A	Genic Upstream Transcript Variant
DNMBP transcript variant 3	NM_001318327.1:c.	N/A	Genic Upstream Transcript Variant
DNMBP transcript variant X1	XM_011539559.3:c.-10-978A… XM_011539559.3:c.-10-978AAAT[4]	N/A	Intron Variant
DNMBP transcript variant X2	XM_047424910.1:c.-10-978A… XM_047424910.1:c.-10-978AAAT[4]	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	(ATTT)₈=	del(ATTT)₄	del(ATTT)₃	del(ATTT)₂	delATTT	dupATTT	dup(ATTT)₂	dup(ATTT)₃	dup(ATTT)₄	dup(ATTT)₅	dup(ATTT)₆	dup(ATTT)₇	dup(ATTT)₈	ins(ATTT)₉
GRCh38.p14 chr 10	NC_000010.11:g.99973081_99973112=	NC_000010.11:g.99973081ATTT[4]	NC_000010.11:g.99973081ATTT[5]	NC_000010.11:g.99973081ATTT[6]	NC_000010.11:g.99973081ATTT[7]	NC_000010.11:g.99973081ATTT[9]	NC_000010.11:g.99973081ATTT[10]	NC_000010.11:g.99973081ATTT[11]	NC_000010.11:g.99973081ATTT[12]	NC_000010.11:g.99973081ATTT[13]	NC_000010.11:g.99973081ATTT[14]	NC_000010.11:g.99973081ATTT[15]	NC_000010.11:g.99973081ATTT[16]	NC_000010.11:g.99973081ATTT[17]
GRCh37.p13 chr 10	NC_000010.10:g.101732838_101732869=	NC_000010.10:g.101732838ATTT[4]	NC_000010.10:g.101732838ATTT[5]	NC_000010.10:g.101732838ATTT[6]	NC_000010.10:g.101732838ATTT[7]	NC_000010.10:g.101732838ATTT[9]	NC_000010.10:g.101732838ATTT[10]	NC_000010.10:g.101732838ATTT[11]	NC_000010.10:g.101732838ATTT[12]	NC_000010.10:g.101732838ATTT[13]	NC_000010.10:g.101732838ATTT[14]	NC_000010.10:g.101732838ATTT[15]	NC_000010.10:g.101732838ATTT[16]	NC_000010.10:g.101732838ATTT[17]
DNMBP transcript	NM_015221.2:c.-10-947=	NM_015221.2:c.-10-978AAAT[4]	NM_015221.2:c.-10-978AAAT[5]	NM_015221.2:c.-10-978AAAT[6]	NM_015221.2:c.-10-978AAAT[7]	NM_015221.2:c.-10-978AAAT[9]	NM_015221.2:c.-10-978AAAT[10]	NM_015221.2:c.-10-978AAAT[11]	NM_015221.2:c.-10-978AAAT[12]	NM_015221.2:c.-10-978AAAT[13]	NM_015221.2:c.-10-978AAAT[14]	NM_015221.2:c.-10-978AAAT[15]	NM_015221.2:c.-10-978AAAT[16]	NM_015221.2:c.-10-978AAAT[17]
DNMBP transcript variant 1	NM_015221.4:c.-10-947=	NM_015221.4:c.-10-978AAAT[4]	NM_015221.4:c.-10-978AAAT[5]	NM_015221.4:c.-10-978AAAT[6]	NM_015221.4:c.-10-978AAAT[7]	NM_015221.4:c.-10-978AAAT[9]	NM_015221.4:c.-10-978AAAT[10]	NM_015221.4:c.-10-978AAAT[11]	NM_015221.4:c.-10-978AAAT[12]	NM_015221.4:c.-10-978AAAT[13]	NM_015221.4:c.-10-978AAAT[14]	NM_015221.4:c.-10-978AAAT[15]	NM_015221.4:c.-10-978AAAT[16]	NM_015221.4:c.-10-978AAAT[17]
DNMBP transcript variant X1	XM_011539559.3:c.-10-947=	XM_011539559.3:c.-10-978AAAT[4]	XM_011539559.3:c.-10-978AAAT[5]	XM_011539559.3:c.-10-978AAAT[6]	XM_011539559.3:c.-10-978AAAT[7]	XM_011539559.3:c.-10-978AAAT[9]	XM_011539559.3:c.-10-978AAAT[10]	XM_011539559.3:c.-10-978AAAT[11]	XM_011539559.3:c.-10-978AAAT[12]	XM_011539559.3:c.-10-978AAAT[13]	XM_011539559.3:c.-10-978AAAT[14]	XM_011539559.3:c.-10-978AAAT[15]	XM_011539559.3:c.-10-978AAAT[16]	XM_011539559.3:c.-10-978AAAT[17]
DNMBP transcript variant X2	XM_047424910.1:c.-10-947=	XM_047424910.1:c.-10-978AAAT[4]	XM_047424910.1:c.-10-978AAAT[5]	XM_047424910.1:c.-10-978AAAT[6]	XM_047424910.1:c.-10-978AAAT[7]	XM_047424910.1:c.-10-978AAAT[9]	XM_047424910.1:c.-10-978AAAT[10]	XM_047424910.1:c.-10-978AAAT[11]	XM_047424910.1:c.-10-978AAAT[12]	XM_047424910.1:c.-10-978AAAT[13]	XM_047424910.1:c.-10-978AAAT[14]	XM_047424910.1:c.-10-978AAAT[15]	XM_047424910.1:c.-10-978AAAT[16]	XM_047424910.1:c.-10-978AAAT[17]

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#.

70 SubSNP, 33 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss39727534	Mar 14, 2006 (126)
2	HUMANGENOME_JCVI	ss95550632	Feb 03, 2009 (130)
3	BCMHGSC_JDW	ss103514654	Dec 01, 2009 (131)
4	BUSHMAN	ss193201044	Jul 04, 2010 (132)
5	GMI	ss287864674	Dec 06, 2013 (138)
6	GMI	ss289033656	May 04, 2012 (137)
7	GMI	ss289033657	May 04, 2012 (138)
8	PJP	ss294672798	May 09, 2011 (135)
9	PJP	ss294672799	May 09, 2011 (137)
10	1000GENOMES	ss327272776	May 09, 2011 (134)
11	1000GENOMES	ss327355205	Jan 10, 2018 (151)
12	1000GENOMES	ss327745437	Jan 10, 2018 (151)
13	LUNTER	ss552060606	Apr 25, 2013 (138)
14	LUNTER	ss552310136	Apr 25, 2013 (138)
15	LUNTER	ss553424734	Apr 25, 2013 (138)
16	SSMP	ss663946372	Apr 01, 2015 (144)
17	1000GENOMES	ss1370003203	Aug 21, 2014 (142)
18	EVA_UK10K_ALSPAC	ss1706870839	Apr 01, 2015 (144)
19	EVA_UK10K_TWINSUK	ss1706870896	Apr 01, 2015 (144)
20	EVA_UK10K_TWINSUK	ss1710484445	Apr 01, 2015 (144)
21	EVA_UK10K_ALSPAC	ss1710484446	Apr 01, 2015 (144)
22	SWEGEN	ss3007026098	Nov 08, 2017 (151)
23	MCHAISSO	ss3064488428	Nov 08, 2017 (151)
24	URBANLAB	ss3649450131	Oct 12, 2018 (152)
25	PACBIO	ss3786766745	Jul 13, 2019 (153)
26	PACBIO	ss3791932376	Jul 13, 2019 (153)
27	PACBIO	ss3796814468	Jul 13, 2019 (153)
28	KHV_HUMAN_GENOMES	ss3813876364	Jul 13, 2019 (153)
29	KHV_HUMAN_GENOMES	ss3813876365	Jul 13, 2019 (153)
30	KHV_HUMAN_GENOMES	ss3813876366	Jul 13, 2019 (153)
31	EVA	ss3839689121	Apr 26, 2020 (154)
32	EVA	ss3845163019	Apr 26, 2020 (154)
33	GNOMAD	ss4224266827	Apr 26, 2021 (155)
34	GNOMAD	ss4224266828	Apr 26, 2021 (155)
35	GNOMAD	ss4224266829	Apr 26, 2021 (155)
36	GNOMAD	ss4224266830	Apr 26, 2021 (155)
37	GNOMAD	ss4224266831	Apr 26, 2021 (155)
38	GNOMAD	ss4224266832	Apr 26, 2021 (155)
39	GNOMAD	ss4224266833	Apr 26, 2021 (155)
40	GNOMAD	ss4224266834	Apr 26, 2021 (155)
41	GNOMAD	ss4224266835	Apr 26, 2021 (155)
42	GNOMAD	ss4224266836	Apr 26, 2021 (155)
43	GNOMAD	ss4224266837	Apr 26, 2021 (155)
44	GNOMAD	ss4224266838	Apr 26, 2021 (155)
45	GNOMAD	ss4224266839	Apr 26, 2021 (155)
46	TOPMED	ss4863861771	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5199133071	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5199133072	Apr 26, 2021 (155)
49	TOMMO_GENOMICS	ss5199133073	Apr 26, 2021 (155)
50	TOMMO_GENOMICS	ss5199133074	Apr 26, 2021 (155)
51	TOMMO_GENOMICS	ss5199133075	Apr 26, 2021 (155)
52	1000G_HIGH_COVERAGE	ss5285210981	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5285210982	Oct 16, 2022 (156)
54	1000G_HIGH_COVERAGE	ss5285210983	Oct 16, 2022 (156)
55	1000G_HIGH_COVERAGE	ss5285210984	Oct 16, 2022 (156)
56	1000G_HIGH_COVERAGE	ss5285210985	Oct 16, 2022 (156)
57	1000G_HIGH_COVERAGE	ss5285210986	Oct 16, 2022 (156)
58	HUGCELL_USP	ss5480657104	Oct 16, 2022 (156)
59	HUGCELL_USP	ss5480657105	Oct 16, 2022 (156)
60	HUGCELL_USP	ss5480657106	Oct 16, 2022 (156)
61	HUGCELL_USP	ss5480657107	Oct 16, 2022 (156)
62	HUGCELL_USP	ss5480657108	Oct 16, 2022 (156)
63	TOMMO_GENOMICS	ss5745399505	Oct 16, 2022 (156)
64	TOMMO_GENOMICS	ss5745399506	Oct 16, 2022 (156)
65	TOMMO_GENOMICS	ss5745399507	Oct 16, 2022 (156)
66	TOMMO_GENOMICS	ss5745399508	Oct 16, 2022 (156)
67	TOMMO_GENOMICS	ss5745399509	Oct 16, 2022 (156)
68	EVA	ss5824856791	Oct 16, 2022 (156)
69	EVA	ss5824856792	Oct 16, 2022 (156)
70	EVA	ss5880227634	Oct 16, 2022 (156)
71	1000Genomes	NC_000010.10 - 101732838	Oct 12, 2018 (152)
72	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28430178 (NC_000010.10:101732837::ATTT 1378/3854) Row 28430179 (NC_000010.10:101732837:ATTT: 1856/3854)	-	Oct 12, 2018 (152)
73	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 28430178 (NC_000010.10:101732837::ATTT 1378/3854) Row 28430179 (NC_000010.10:101732837:ATTT: 1856/3854)	-	Oct 12, 2018 (152)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 361773882 (NC_000010.11:99973080::ATTT 35233/137648) Row 361773883 (NC_000010.11:99973080::ATTTATTT 9989/137788) Row 361773884 (NC_000010.11:99973080::ATTTATTTATTT 450/137858)...	-	Apr 26, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 57102378 (NC_000010.10:101732837::ATTTATTT 1347/16760) Row 57102379 (NC_000010.10:101732837:ATTT: 3721/16760) Row 57102380 (NC_000010.10:101732837::ATTT 4625/16760)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 57102378 (NC_000010.10:101732837::ATTTATTT 1347/16760) Row 57102379 (NC_000010.10:101732837:ATTT: 3721/16760) Row 57102380 (NC_000010.10:101732837::ATTT 4625/16760)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 57102378 (NC_000010.10:101732837::ATTTATTT 1347/16760) Row 57102379 (NC_000010.10:101732837:ATTT: 3721/16760) Row 57102380 (NC_000010.10:101732837::ATTT 4625/16760)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 57102378 (NC_000010.10:101732837::ATTTATTT 1347/16760) Row 57102379 (NC_000010.10:101732837:ATTT: 3721/16760) Row 57102380 (NC_000010.10:101732837::ATTT 4625/16760)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 57102378 (NC_000010.10:101732837::ATTTATTT 1347/16760) Row 57102379 (NC_000010.10:101732837:ATTT: 3721/16760) Row 57102380 (NC_000010.10:101732837::ATTT 4625/16760)...	-	Apr 26, 2021 (155)
92	14KJPN Submission ignored due to conflicting rows: Row 79236609 (NC_000010.11:99973080:ATTT: 6293/28258) Row 79236610 (NC_000010.11:99973080::ATTTATTT 2196/28258) Row 79236611 (NC_000010.11:99973080::ATTT 7757/28258)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 79236609 (NC_000010.11:99973080:ATTT: 6293/28258) Row 79236610 (NC_000010.11:99973080::ATTTATTT 2196/28258) Row 79236611 (NC_000010.11:99973080::ATTT 7757/28258)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 79236609 (NC_000010.11:99973080:ATTT: 6293/28258) Row 79236610 (NC_000010.11:99973080::ATTTATTT 2196/28258) Row 79236611 (NC_000010.11:99973080::ATTT 7757/28258)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 79236609 (NC_000010.11:99973080:ATTT: 6293/28258) Row 79236610 (NC_000010.11:99973080::ATTTATTT 2196/28258) Row 79236611 (NC_000010.11:99973080::ATTT 7757/28258)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 79236609 (NC_000010.11:99973080:ATTT: 6293/28258) Row 79236610 (NC_000010.11:99973080::ATTTATTT 2196/28258) Row 79236611 (NC_000010.11:99973080::ATTT 7757/28258)...	-	Oct 16, 2022 (156)
97	TopMed	NC_000010.11 - 99973081	Apr 26, 2021 (155)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28430178 (NC_000010.10:101732837::ATTT 1340/3708) Row 28430179 (NC_000010.10:101732837:ATTT: 1788/3708)	-	Oct 12, 2018 (152)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 28430178 (NC_000010.10:101732837::ATTT 1340/3708) Row 28430179 (NC_000010.10:101732837:ATTT: 1788/3708)	-	Oct 12, 2018 (152)
100	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 6312322 (NC_000010.10:101732837::ATTT 48/143) Row 6312323 (NC_000010.10:101732837::ATTTATTT 22/117) Row 6312324 (NC_000010.10:101732837:ATTT: 49/144)	-	Jul 13, 2019 (153)
101	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 6312322 (NC_000010.10:101732837::ATTT 48/143) Row 6312323 (NC_000010.10:101732837::ATTTATTT 22/117) Row 6312324 (NC_000010.10:101732837:ATTT: 49/144)	-	Jul 13, 2019 (153)
102	A Vietnamese Genetic Variation Database Submission ignored due to conflicting rows: Row 6312322 (NC_000010.10:101732837::ATTT 48/143) Row 6312323 (NC_000010.10:101732837::ATTTATTT 22/117) Row 6312324 (NC_000010.10:101732837:ATTT: 49/144)	-	Jul 13, 2019 (153)
103	ALFA	NC_000010.11 - 99973081	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).

Associated ID	History Updated (Build)
rs150806863	May 15, 2013 (138)
rs144378724	May 11, 2012 (137)
rs149623633	Sep 17, 2011 (135)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4224266839	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTT	(self)
ss4224266838, ss5285210985, ss5480657107	NC_000010.11:99973080:ATTTATTTATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTT	(self)
ss5199133075	NC_000010.10:101732837:ATTTATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTT	(self)
ss4224266837, ss5745399509	NC_000010.11:99973080:ATTTATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTT	(self)
ss289033656, ss294672798, ss327355205, ss327745437, ss552310136, ss553424734	NC_000010.9:101722827:ATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
ss294672799	NC_000010.9:101722855:ATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
51201677, ss663946372, ss1370003203, ss1706870839, ss1706870896, ss3007026098, ss3786766745, ss3791932376, ss3796814468, ss5199133072, ss5824856791	NC_000010.10:101732837:ATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
ss3064488428, ss3813876365, ss4224266836, ss5285210981, ss5480657104, ss5745399505, ss5880227634	NC_000010.11:99973080:ATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
ss3649450131	NC_000010.11:99973100:ATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
ss39727534, ss95550632, ss103514654	NT_030059.13:52537329:ATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
ss193201044	NT_030059.14:58279559:ATTT:	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTT	(self)
ss327272776, ss552060606	NC_000010.9:101722827::ATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss289033657	NC_000010.9:101722859::ATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss5199133073, ss5824856792	NC_000010.10:101732837::ATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss1710484445, ss1710484446, ss3839689121	NC_000010.10:101732841::ATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266827, ss5285210982, ss5480657105, ss5745399507	NC_000010.11:99973080::ATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss3813876366, ss3845163019	NC_000010.11:99973084::ATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss287864674	NT_030059.13:52537333::ATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss5199133071	NC_000010.10:101732837::ATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266828, ss5285210983, ss5480657106, ss5745399506	NC_000010.11:99973080::ATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss3813876364	NC_000010.11:99973084::ATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss5199133074	NC_000010.10:101732837::ATTTATTTAT… NC_000010.10:101732837::ATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266829, ss5285210986, ss5480657108, ss5745399508	NC_000010.11:99973080::ATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
79407426, ss4224266830, ss4863861771	NC_000010.11:99973080::ATTTATTTATT… NC_000010.11:99973080::ATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266831, ss5285210984	NC_000010.11:99973080::ATTTATTTATT… NC_000010.11:99973080::ATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266832	NC_000010.11:99973080::ATTTATTTATT… NC_000010.11:99973080::ATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266833	NC_000010.11:99973080::ATTTATTTATT… NC_000010.11:99973080::ATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
2734698147	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266834	NC_000010.11:99973080::ATTTATTTATT… NC_000010.11:99973080::ATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(self)
ss4224266835	NC_000010.11:99973080::ATTTATTTATT… NC_000010.11:99973080::ATTTATTTATTTATTTATTTATTTATTTATTTATTT	NC_000010.11:99973080:ATTTATTTATTT… NC_000010.11:99973080:ATTTATTTATTTATTTATTTATTTATTTATTT:ATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTT	(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 rs35399198

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
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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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs35399198