Name: rs1491542420
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.

rs1491542420

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:29450779-29450780 (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: insA / insATA / insATATA / ins(AT)…
insA / insATA / insATATA / ins(AT)₃A / ins(AT)₄A / ins(AT)₅A / ins(AT)₆A / ins(AT)₇A / insATG / insG
Variation Type: Insertion
Frequency: insA=0.00000 (0/11110, ALFA)
insATA=0.00000 (0/11110, ALFA)
insATATA=0.00000 (0/11110, ALFA) (+ 5 more)
ins(AT)₃A=0.00000 (0/11110, ALFA)
ins(AT)₄A=0.00000 (0/11110, ALFA)
ins(AT)₆A=0.00000 (0/11110, ALFA)
insATG=0.00000 (0/11110, ALFA)
insG=0.00000 (0/11110, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: BOLA2-SMG1P6 : 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	HWEP
Total	Global	11110	=1.00000	A=0.00000, ATA=0.00000, ATATA=0.00000, ATATATA=0.00000, ATATATATA=0.00000, ATATATATATATA=0.00000, ATG=0.00000, G=0.00000	1.0	N/A
European	Sub	7008	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATATA=0.0000, ATG=0.0000, G=0.0000	1.0	N/A
African	Sub	2714	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATATA=0.0000, ATG=0.0000, G=0.0000	1.0	N/A
African Others	Sub	108	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, ATG=0.000, G=0.000	1.0	N/A
African American	Sub	2606	=1.0000	A=0.0000, ATA=0.0000, ATATA=0.0000, ATATATA=0.0000, ATATATATA=0.0000, ATATATATATATA=0.0000, ATG=0.0000, G=0.0000	1.0	N/A
Asian	Sub	100	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATATA=0.00, ATG=0.00, G=0.00	1.0	N/A
East Asian	Sub	76	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATATA=0.00, ATG=0.00, G=0.00	1.0	N/A
Other Asian	Sub	24	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATATA=0.00, ATG=0.00, G=0.00	1.0	N/A
Latin American 1	Sub	142	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, ATG=0.000, G=0.000	1.0	N/A
Latin American 2	Sub	600	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, ATG=0.000, G=0.000	1.0	N/A
South Asian	Sub	90	=1.00	A=0.00, ATA=0.00, ATATA=0.00, ATATATA=0.00, ATATATATA=0.00, ATATATATATATA=0.00, ATG=0.00, G=0.00	1.0	N/A
Other	Sub	456	=1.000	A=0.000, ATA=0.000, ATATA=0.000, ATATATA=0.000, ATATATATA=0.000, ATATATATATATA=0.000, ATG=0.000, G=0.000	1.0	N/A

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	11110	- No frequency provided	insA=0.00000, insATA=0.00000, insATATA=0.00000, ins(AT)₃A=0.00000, ins(AT)₄A=0.00000, ins(AT)₆A=0.00000, insATG=0.00000, insG=0.00000
Allele Frequency Aggregator	European	Sub	7008	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₆A=0.0000, insATG=0.0000, insG=0.0000
Allele Frequency Aggregator	African	Sub	2714	- No frequency provided	insA=0.0000, insATA=0.0000, insATATA=0.0000, ins(AT)₃A=0.0000, ins(AT)₄A=0.0000, ins(AT)₆A=0.0000, insATG=0.0000, insG=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	600	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₆A=0.000, insATG=0.000, insG=0.000
Allele Frequency Aggregator	Other	Sub	456	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₆A=0.000, insATG=0.000, insG=0.000
Allele Frequency Aggregator	Latin American 1	Sub	142	- No frequency provided	insA=0.000, insATA=0.000, insATATA=0.000, ins(AT)₃A=0.000, ins(AT)₄A=0.000, ins(AT)₆A=0.000, insATG=0.000, insG=0.000
Allele Frequency Aggregator	Asian	Sub	100	- No frequency provided	insA=0.00, insATA=0.00, insATATA=0.00, ins(AT)₃A=0.00, ins(AT)₄A=0.00, ins(AT)₆A=0.00, insATG=0.00, insG=0.00
Allele Frequency Aggregator	South Asian	Sub	90	- No frequency provided	insA=0.00, insATA=0.00, insATATA=0.00, ins(AT)₃A=0.00, ins(AT)₄A=0.00, ins(AT)₆A=0.00, insATG=0.00, insG=0.00

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 16	NC_000016.10:g.29450779_29450780insA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATATA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATATATA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATATATATA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATATATATATA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATATATATATATA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATATATATATATATA
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insATG
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780insG
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATATA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATATATA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATATATATA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATATATATATA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATATATATATATA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATATATATATATATA
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insATG
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101insG

Gene: BOLA2-SMG1P6, BOLA2-SMG1P6 readthrough (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
BOLA2-SMG1P6 transcript variant 1	NM_001320622.1:c.321+3236… NM_001320622.1:c.321+3236_321+3237insT	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 2	NM_001320623.1:c.359+3236… NM_001320623.1:c.359+3236_359+3237insT	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 3	NM_001320624.1:c.261+3411… NM_001320624.1:c.261+3411_261+3412insT	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 4	NM_001320625.1:c.5+3411_5… NM_001320625.1:c.5+3411_5+3412insT	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 5	NM_001320627.1:c.-16+3236… NM_001320627.1:c.-16+3236_-16+3237insT	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 6	NM_001320628.1:c.-16+3236… NM_001320628.1:c.-16+3236_-16+3237insT	N/A	Intron Variant
BOLA2-SMG1P6 transcript variant 7	NR_135316.1:n.	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	=	insA	insATA	insATATA	ins(AT)₃A	ins(AT)₄A	ins(AT)₅A	ins(AT)₆A	ins(AT)₇A	insATG	insG
GRCh38.p14 chr 16	NC_000016.10:g.29450779_29450780=	NC_000016.10:g.29450779_29450780insA	NC_000016.10:g.29450779_29450780insATA	NC_000016.10:g.29450779_29450780insATATA	NC_000016.10:g.29450779_29450780insATATATA	NC_000016.10:g.29450779_29450780insATATATATA	NC_000016.10:g.29450779_29450780insATATATATATA	NC_000016.10:g.29450779_29450780insATATATATATATA	NC_000016.10:g.29450779_29450780insATATATATATATATA	NC_000016.10:g.29450779_29450780insATG	NC_000016.10:g.29450779_29450780insG
GRCh37.p13 chr 16	NC_000016.9:g.29462100_29462101=	NC_000016.9:g.29462100_29462101insA	NC_000016.9:g.29462100_29462101insATA	NC_000016.9:g.29462100_29462101insATATA	NC_000016.9:g.29462100_29462101insATATATA	NC_000016.9:g.29462100_29462101insATATATATA	NC_000016.9:g.29462100_29462101insATATATATATA	NC_000016.9:g.29462100_29462101insATATATATATATA	NC_000016.9:g.29462100_29462101insATATATATATATATA	NC_000016.9:g.29462100_29462101insATG	NC_000016.9:g.29462100_29462101insG
BOLA2-SMG1P6 transcript variant 1	NM_001320622.1:c.321+3236=	NM_001320622.1:c.321+3236_321+3237insT	NM_001320622.1:c.321+3236_321+3237insTAT	NM_001320622.1:c.321+3236_321+3237insTATAT	NM_001320622.1:c.321+3236_321+3237insTATATAT	NM_001320622.1:c.321+3236_321+3237insTATATATAT	NM_001320622.1:c.321+3236_321+3237insTATATATATAT	NM_001320622.1:c.321+3236_321+3237insTATATATATATAT	NM_001320622.1:c.321+3236_321+3237insTATATATATATATAT	NM_001320622.1:c.321+3236_321+3237insCAT	NM_001320622.1:c.321+3236_321+3237insC
BOLA2-SMG1P6 transcript variant 2	NM_001320623.1:c.359+3236=	NM_001320623.1:c.359+3236_359+3237insT	NM_001320623.1:c.359+3236_359+3237insTAT	NM_001320623.1:c.359+3236_359+3237insTATAT	NM_001320623.1:c.359+3236_359+3237insTATATAT	NM_001320623.1:c.359+3236_359+3237insTATATATAT	NM_001320623.1:c.359+3236_359+3237insTATATATATAT	NM_001320623.1:c.359+3236_359+3237insTATATATATATAT	NM_001320623.1:c.359+3236_359+3237insTATATATATATATAT	NM_001320623.1:c.359+3236_359+3237insCAT	NM_001320623.1:c.359+3236_359+3237insC
BOLA2-SMG1P6 transcript variant 3	NM_001320624.1:c.261+3411=	NM_001320624.1:c.261+3411_261+3412insT	NM_001320624.1:c.261+3411_261+3412insTAT	NM_001320624.1:c.261+3411_261+3412insTATAT	NM_001320624.1:c.261+3411_261+3412insTATATAT	NM_001320624.1:c.261+3411_261+3412insTATATATAT	NM_001320624.1:c.261+3411_261+3412insTATATATATAT	NM_001320624.1:c.261+3411_261+3412insTATATATATATAT	NM_001320624.1:c.261+3411_261+3412insTATATATATATATAT	NM_001320624.1:c.261+3411_261+3412insCAT	NM_001320624.1:c.261+3411_261+3412insC
BOLA2-SMG1P6 transcript variant 4	NM_001320625.1:c.5+3411=	NM_001320625.1:c.5+3411_5+3412insT	NM_001320625.1:c.5+3411_5+3412insTAT	NM_001320625.1:c.5+3411_5+3412insTATAT	NM_001320625.1:c.5+3411_5+3412insTATATAT	NM_001320625.1:c.5+3411_5+3412insTATATATAT	NM_001320625.1:c.5+3411_5+3412insTATATATATAT	NM_001320625.1:c.5+3411_5+3412insTATATATATATAT	NM_001320625.1:c.5+3411_5+3412insTATATATATATATAT	NM_001320625.1:c.5+3411_5+3412insCAT	NM_001320625.1:c.5+3411_5+3412insC
BOLA2-SMG1P6 transcript variant 5	NM_001320627.1:c.-16+3236=	NM_001320627.1:c.-16+3236_-16+3237insT	NM_001320627.1:c.-16+3236_-16+3237insTAT	NM_001320627.1:c.-16+3236_-16+3237insTATAT	NM_001320627.1:c.-16+3236_-16+3237insTATATAT	NM_001320627.1:c.-16+3236_-16+3237insTATATATAT	NM_001320627.1:c.-16+3236_-16+3237insTATATATATAT	NM_001320627.1:c.-16+3236_-16+3237insTATATATATATAT	NM_001320627.1:c.-16+3236_-16+3237insTATATATATATATAT	NM_001320627.1:c.-16+3236_-16+3237insCAT	NM_001320627.1:c.-16+3236_-16+3237insC
BOLA2-SMG1P6 transcript variant 6	NM_001320628.1:c.-16+3236=	NM_001320628.1:c.-16+3236_-16+3237insT	NM_001320628.1:c.-16+3236_-16+3237insTAT	NM_001320628.1:c.-16+3236_-16+3237insTATAT	NM_001320628.1:c.-16+3236_-16+3237insTATATAT	NM_001320628.1:c.-16+3236_-16+3237insTATATATAT	NM_001320628.1:c.-16+3236_-16+3237insTATATATATAT	NM_001320628.1:c.-16+3236_-16+3237insTATATATATATAT	NM_001320628.1:c.-16+3236_-16+3237insTATATATATATATAT	NM_001320628.1:c.-16+3236_-16+3237insCAT	NM_001320628.1:c.-16+3236_-16+3237insC
BOLA2 transcript variant X1	XM_005255415.1:c.359+3236=	XM_005255415.1:c.359+3236_359+3237insT	XM_005255415.1:c.359+3236_359+3237insTAT	XM_005255415.1:c.359+3236_359+3237insTATAT	XM_005255415.1:c.359+3236_359+3237insTATATAT	XM_005255415.1:c.359+3236_359+3237insTATATATAT	XM_005255415.1:c.359+3236_359+3237insTATATATATAT	XM_005255415.1:c.359+3236_359+3237insTATATATATATAT	XM_005255415.1:c.359+3236_359+3237insTATATATATATATAT	XM_005255415.1:c.359+3236_359+3237insCAT	XM_005255415.1:c.359+3236_359+3237insC
BOLA2 transcript variant X2	XM_005255416.1:c.-16+3236=	XM_005255416.1:c.-16+3236_-16+3237insT	XM_005255416.1:c.-16+3236_-16+3237insTAT	XM_005255416.1:c.-16+3236_-16+3237insTATAT	XM_005255416.1:c.-16+3236_-16+3237insTATATAT	XM_005255416.1:c.-16+3236_-16+3237insTATATATAT	XM_005255416.1:c.-16+3236_-16+3237insTATATATATAT	XM_005255416.1:c.-16+3236_-16+3237insTATATATATATAT	XM_005255416.1:c.-16+3236_-16+3237insTATATATATATATAT	XM_005255416.1:c.-16+3236_-16+3237insCAT	XM_005255416.1:c.-16+3236_-16+3237insC

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#.

23 SubSNP, 18 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3699120541	Jul 13, 2019 (153)
2	EVA_DECODE	ss3699120542	Jul 13, 2019 (153)
3	EVA_DECODE	ss3699120543	Jul 13, 2019 (153)
4	EVA_DECODE	ss3699120544	Jul 13, 2019 (153)
5	EVA_DECODE	ss3699120545	Jul 13, 2019 (153)
6	PACBIO	ss3788019908	Jul 13, 2019 (153)
7	KOGIC	ss3977386985	Apr 27, 2020 (154)
8	KOGIC	ss3977386986	Apr 27, 2020 (154)
9	GNOMAD	ss4299340478	Apr 26, 2021 (155)
10	GNOMAD	ss4299340479	Apr 26, 2021 (155)
11	GNOMAD	ss4299340480	Apr 26, 2021 (155)
12	GNOMAD	ss4299340481	Apr 26, 2021 (155)
13	GNOMAD	ss4299340482	Apr 26, 2021 (155)
14	GNOMAD	ss4299340483	Apr 26, 2021 (155)
15	GNOMAD	ss4299340484	Apr 26, 2021 (155)
16	TOMMO_GENOMICS	ss5219140990	Apr 26, 2021 (155)
17	TOMMO_GENOMICS	ss5219140991	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5219140992	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5219140993	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5773830297	Oct 16, 2022 (156)
21	TOMMO_GENOMICS	ss5773830298	Oct 16, 2022 (156)
22	TOMMO_GENOMICS	ss5773830299	Oct 16, 2022 (156)
23	TOMMO_GENOMICS	ss5773830300	Oct 16, 2022 (156)
24	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002364 (NC_000016.10:29450779::A 1735/18202) Row 487002365 (NC_000016.10:29450779::ATA 163/18756) Row 487002366 (NC_000016.10:29450779::ATATA 165/18748)...	-	Apr 26, 2021 (155)
25	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002364 (NC_000016.10:29450779::A 1735/18202) Row 487002365 (NC_000016.10:29450779::ATA 163/18756) Row 487002366 (NC_000016.10:29450779::ATATA 165/18748)...	-	Apr 26, 2021 (155)
26	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002364 (NC_000016.10:29450779::A 1735/18202) Row 487002365 (NC_000016.10:29450779::ATA 163/18756) Row 487002366 (NC_000016.10:29450779::ATATA 165/18748)...	-	Apr 26, 2021 (155)
27	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002364 (NC_000016.10:29450779::A 1735/18202) Row 487002365 (NC_000016.10:29450779::ATA 163/18756) Row 487002366 (NC_000016.10:29450779::ATATA 165/18748)...	-	Apr 26, 2021 (155)
28	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002364 (NC_000016.10:29450779::A 1735/18202) Row 487002365 (NC_000016.10:29450779::ATA 163/18756) Row 487002366 (NC_000016.10:29450779::ATATA 165/18748)...	-	Apr 26, 2021 (155)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002364 (NC_000016.10:29450779::A 1735/18202) Row 487002365 (NC_000016.10:29450779::ATA 163/18756) Row 487002366 (NC_000016.10:29450779::ATATA 165/18748)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 487002364 (NC_000016.10:29450779::A 1735/18202) Row 487002365 (NC_000016.10:29450779::ATA 163/18756) Row 487002366 (NC_000016.10:29450779::ATATA 165/18748)...	-	Apr 26, 2021 (155)
31	Korean Genome Project Submission ignored due to conflicting rows: Row 33764986 (NC_000016.10:29450779::A 103/1358) Row 33764987 (NC_000016.10:29450779::ATA 13/1358)	-	Apr 27, 2020 (154)
32	Korean Genome Project Submission ignored due to conflicting rows: Row 33764986 (NC_000016.10:29450779::A 103/1358) Row 33764987 (NC_000016.10:29450779::ATA 13/1358)	-	Apr 27, 2020 (154)
33	8.3KJPN Submission ignored due to conflicting rows: Row 77110297 (NC_000016.9:29462100::A 1516/14194) Row 77110298 (NC_000016.9:29462100::ATA 96/14194) Row 77110299 (NC_000016.9:29462100::ATATA 15/14194)...	-	Apr 26, 2021 (155)
34	8.3KJPN Submission ignored due to conflicting rows: Row 77110297 (NC_000016.9:29462100::A 1516/14194) Row 77110298 (NC_000016.9:29462100::ATA 96/14194) Row 77110299 (NC_000016.9:29462100::ATATA 15/14194)...	-	Apr 26, 2021 (155)
35	8.3KJPN Submission ignored due to conflicting rows: Row 77110297 (NC_000016.9:29462100::A 1516/14194) Row 77110298 (NC_000016.9:29462100::ATA 96/14194) Row 77110299 (NC_000016.9:29462100::ATATA 15/14194)...	-	Apr 26, 2021 (155)
36	8.3KJPN Submission ignored due to conflicting rows: Row 77110297 (NC_000016.9:29462100::A 1516/14194) Row 77110298 (NC_000016.9:29462100::ATA 96/14194) Row 77110299 (NC_000016.9:29462100::ATATA 15/14194)...	-	Apr 26, 2021 (155)
37	14KJPN Submission ignored due to conflicting rows: Row 107667401 (NC_000016.10:29450779::A 2231/23896) Row 107667402 (NC_000016.10:29450779::ATA 122/23896) Row 107667403 (NC_000016.10:29450779::ATATA 20/23896)...	-	Oct 16, 2022 (156)
38	14KJPN Submission ignored due to conflicting rows: Row 107667401 (NC_000016.10:29450779::A 2231/23896) Row 107667402 (NC_000016.10:29450779::ATA 122/23896) Row 107667403 (NC_000016.10:29450779::ATATA 20/23896)...	-	Oct 16, 2022 (156)
39	14KJPN Submission ignored due to conflicting rows: Row 107667401 (NC_000016.10:29450779::A 2231/23896) Row 107667402 (NC_000016.10:29450779::ATA 122/23896) Row 107667403 (NC_000016.10:29450779::ATATA 20/23896)...	-	Oct 16, 2022 (156)
40	14KJPN Submission ignored due to conflicting rows: Row 107667401 (NC_000016.10:29450779::A 2231/23896) Row 107667402 (NC_000016.10:29450779::ATA 122/23896) Row 107667403 (NC_000016.10:29450779::ATATA 20/23896)...	-	Oct 16, 2022 (156)
41	ALFA	NC_000016.10 - 29450780	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
ss3788019908, ss5219140990	NC_000016.9:29462100::A	NC_000016.10:29450779::A	(self)
2343297842, ss3699120541, ss3977386985, ss4299340478, ss5773830297	NC_000016.10:29450779::A	NC_000016.10:29450779::A	(self)
ss5219140991	NC_000016.9:29462100::ATA	NC_000016.10:29450779::ATA	(self)
2343297842, ss3699120542, ss3977386986, ss4299340479, ss5773830298	NC_000016.10:29450779::ATA	NC_000016.10:29450779::ATA	(self)
ss5219140992	NC_000016.9:29462100::ATATA	NC_000016.10:29450779::ATATA	(self)
2343297842, ss3699120543, ss4299340480, ss5773830299	NC_000016.10:29450779::ATATA	NC_000016.10:29450779::ATATA	(self)
ss5219140993	NC_000016.9:29462100::ATATATA	NC_000016.10:29450779::ATATATA	(self)
2343297842, ss3699120544, ss4299340481, ss5773830300	NC_000016.10:29450779::ATATATA	NC_000016.10:29450779::ATATATA	(self)
2343297842, ss4299340482	NC_000016.10:29450779::ATATATATA	NC_000016.10:29450779::ATATATATA	(self)
ss3699120545	NC_000016.10:29450779::ATATATATATA	NC_000016.10:29450779::ATATATATATA	(self)
2343297842, ss4299340483	NC_000016.10:29450779::ATATATATATA… NC_000016.10:29450779::ATATATATATATA	NC_000016.10:29450779::ATATATATATA… NC_000016.10:29450779::ATATATATATATA	(self)
ss4299340484	NC_000016.10:29450779::ATATATATATA… NC_000016.10:29450779::ATATATATATATATA	NC_000016.10:29450779::ATATATATATA… NC_000016.10:29450779::ATATATATATATATA	(self)
2343297842	NC_000016.10:29450779::ATG	NC_000016.10:29450779::ATG	(self)
2343297842	NC_000016.10:29450779::G	NC_000016.10:29450779::G	(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 rs1491542420

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

rs1491542420