Name: rs1491374744
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.

rs1491374744

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr15:90909605-90909606 (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: insCT / insCTT / insC(T)₄ / insC(T…
insCT / insCTT / insC(T)₄ / insC(T)₅ / insC(T)₆
Variation Type: Insertion
Frequency: insCT=0.00007 (2/28234, 14KJPN)
insCT=0.00222 (36/16186, ALFA)
insCT=0.010 (6/592, NorthernSweden)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: MAN2A2 : 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	16186	=0.99623	CT=0.00222, CTT=0.00043, CTTTTT=0.00068, CTTTT=0.00043	0.996257	0.000749	0.002994	32
European	Sub	11935	=0.99564	CT=0.00226, CTT=0.00059, CTTTTT=0.00092, CTTTT=0.00059	0.996435	0.001019	0.002547	32
African	Sub	2816	=0.9972	CT=0.0028, CTT=0.0000, CTTTTT=0.0000, CTTTT=0.0000	0.994318	0.0	0.005682	0
African Others	Sub	108	=1.000	CT=0.000, CTT=0.000, CTTTTT=0.000, CTTTT=0.000	1.0	0.0	0.0	N/A
African American	Sub	2708	=0.9970	CT=0.0030, CTT=0.0000, CTTTTT=0.0000, CTTTT=0.0000	0.994092	0.0	0.005908	0
Asian	Sub	108	=1.000	CT=0.000, CTT=0.000, CTTTTT=0.000, CTTTT=0.000	1.0	0.0	0.0	N/A
East Asian	Sub	84	=1.00	CT=0.00, CTT=0.00, CTTTTT=0.00, CTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	24	=1.00	CT=0.00, CTT=0.00, CTTTTT=0.00, CTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	146	=1.000	CT=0.000, CTT=0.000, CTTTTT=0.000, CTTTT=0.000	1.0	0.0	0.0	N/A
Latin American 2	Sub	610	=0.998	CT=0.002, CTT=0.000, CTTTTT=0.000, CTTTT=0.000	0.996721	0.0	0.003279	0
South Asian	Sub	94	=1.00	CT=0.00, CTT=0.00, CTTTTT=0.00, CTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	477	=1.000	CT=0.000, CTT=0.000, CTTTTT=0.000, CTTTT=0.000	1.0	0.0	0.0	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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
14KJPN	JAPANESE	Study-wide	28234	- No frequency provided	insCT=0.00007
Allele Frequency Aggregator	Total	Global	16186	- No frequency provided	insCT=0.00222, insCTT=0.00043, insC(T)₄=0.00043, insC(T)₅=0.00068
Allele Frequency Aggregator	European	Sub	11935	- No frequency provided	insCT=0.00226, insCTT=0.00059, insC(T)₄=0.00059, insC(T)₅=0.00092
Allele Frequency Aggregator	African	Sub	2816	- No frequency provided	insCT=0.0028, insCTT=0.0000, insC(T)₄=0.0000, insC(T)₅=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	610	- No frequency provided	insCT=0.002, insCTT=0.000, insC(T)₄=0.000, insC(T)₅=0.000
Allele Frequency Aggregator	Other	Sub	477	- No frequency provided	insCT=0.000, insCTT=0.000, insC(T)₄=0.000, insC(T)₅=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	- No frequency provided	insCT=0.000, insCTT=0.000, insC(T)₄=0.000, insC(T)₅=0.000
Allele Frequency Aggregator	Asian	Sub	108	- No frequency provided	insCT=0.000, insCTT=0.000, insC(T)₄=0.000, insC(T)₅=0.000
Allele Frequency Aggregator	South Asian	Sub	94	- No frequency provided	insCT=0.00, insCTT=0.00, insC(T)₄=0.00, insC(T)₅=0.00
Northern Sweden	ACPOP	Study-wide	592	- No frequency provided	insCT=0.010

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 15	NC_000015.10:g.90909605_90909606insCT
GRCh38.p14 chr 15	NC_000015.10:g.90909605_90909606insCTT
GRCh38.p14 chr 15	NC_000015.10:g.90909605_90909606insCTTTT
GRCh38.p14 chr 15	NC_000015.10:g.90909605_90909606insCTTTTT
GRCh38.p14 chr 15	NC_000015.10:g.90909605_90909606insCTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.91452835_91452836insCT
GRCh37.p13 chr 15	NC_000015.9:g.91452835_91452836insCTT
GRCh37.p13 chr 15	NC_000015.9:g.91452835_91452836insCTTTT
GRCh37.p13 chr 15	NC_000015.9:g.91452835_91452836insCTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.91452835_91452836insCTTTTTT

Gene: MAN2A2, mannosidase alpha class 2A member 2 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
MAN2A2 transcript variant 2	NM_001320977.2:c.1374+101… NM_001320977.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant 1	NM_006122.4:c.1374+101_13… NM_006122.4:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant 3	NR_135502.2:n.	N/A	Intron Variant
MAN2A2 transcript variant 4	NR_135503.2:n.	N/A	Intron Variant
MAN2A2 transcript variant 5	NR_135504.1:n.	N/A	Intron Variant
MAN2A2 transcript variant X2	XM_005254910.4:c.1374+101… XM_005254910.4:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X5	XM_017022184.2:c.1374+101… XM_017022184.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X9	XM_017022185.2:c.1374+101… XM_017022185.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X3	XM_024449920.2:c.1374+101… XM_024449920.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X1	XM_024449921.2:c.1374+101… XM_024449921.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X7	XM_024449922.2:c.1374+101… XM_024449922.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X6	XM_024449923.2:c.1374+101… XM_024449923.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X8	XM_024449924.2:c.1374+101… XM_024449924.2:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X4	XM_047432507.1:c.1374+101… XM_047432507.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X10	XM_047432508.1:c.1374+101… XM_047432508.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X11	XM_047432509.1:c.1374+101… XM_047432509.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X12	XM_047432510.1:c.1374+101… XM_047432510.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X13	XM_047432511.1:c.1374+101… XM_047432511.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X14	XM_047432512.1:c.1374+101… XM_047432512.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X15	XM_047432513.1:c.1374+101… XM_047432513.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X16	XM_047432514.1:c.1374+101… XM_047432514.1:c.1374+101_1374+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X17	XM_047432515.1:c.314+101_… XM_047432515.1:c.314+101_314+102insCT	N/A	Intron Variant
MAN2A2 transcript variant X18	XM_047432516.1:c.314+101_… XM_047432516.1:c.314+101_314+102insCT	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	=	insCT	insCTT	insC(T)₄	insC(T)₅	insC(T)₆
GRCh38.p14 chr 15	NC_000015.10:g.90909605_90909606=	NC_000015.10:g.90909605_90909606insCT	NC_000015.10:g.90909605_90909606insCTT	NC_000015.10:g.90909605_90909606insCTTTT	NC_000015.10:g.90909605_90909606insCTTTTT	NC_000015.10:g.90909605_90909606insCTTTTTT
GRCh37.p13 chr 15	NC_000015.9:g.91452835_91452836=	NC_000015.9:g.91452835_91452836insCT	NC_000015.9:g.91452835_91452836insCTT	NC_000015.9:g.91452835_91452836insCTTTT	NC_000015.9:g.91452835_91452836insCTTTTT	NC_000015.9:g.91452835_91452836insCTTTTTT
MAN2A2 transcript variant 2	NM_001320977.2:c.1374+102=	NM_001320977.2:c.1374+101_1374+102insCT	NM_001320977.2:c.1374+101_1374+102insCTT	NM_001320977.2:c.1374+101_1374+102insCTTTT	NM_001320977.2:c.1374+101_1374+102insCTTTTT	NM_001320977.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript	NM_006122.2:c.1374+102=	NM_006122.2:c.1374+101_1374+102insCT	NM_006122.2:c.1374+101_1374+102insCTT	NM_006122.2:c.1374+101_1374+102insCTTTT	NM_006122.2:c.1374+101_1374+102insCTTTTT	NM_006122.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant 1	NM_006122.4:c.1374+102=	NM_006122.4:c.1374+101_1374+102insCT	NM_006122.4:c.1374+101_1374+102insCTT	NM_006122.4:c.1374+101_1374+102insCTTTT	NM_006122.4:c.1374+101_1374+102insCTTTTT	NM_006122.4:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X1	XM_005254910.1:c.1374+102=	XM_005254910.1:c.1374+101_1374+102insCT	XM_005254910.1:c.1374+101_1374+102insCTT	XM_005254910.1:c.1374+101_1374+102insCTTTT	XM_005254910.1:c.1374+101_1374+102insCTTTTT	XM_005254910.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X2	XM_005254910.4:c.1374+102=	XM_005254910.4:c.1374+101_1374+102insCT	XM_005254910.4:c.1374+101_1374+102insCTT	XM_005254910.4:c.1374+101_1374+102insCTTTT	XM_005254910.4:c.1374+101_1374+102insCTTTTT	XM_005254910.4:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X2	XM_005254911.1:c.1374+102=	XM_005254911.1:c.1374+101_1374+102insCT	XM_005254911.1:c.1374+101_1374+102insCTT	XM_005254911.1:c.1374+101_1374+102insCTTTT	XM_005254911.1:c.1374+101_1374+102insCTTTTT	XM_005254911.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X5	XM_017022184.2:c.1374+102=	XM_017022184.2:c.1374+101_1374+102insCT	XM_017022184.2:c.1374+101_1374+102insCTT	XM_017022184.2:c.1374+101_1374+102insCTTTT	XM_017022184.2:c.1374+101_1374+102insCTTTTT	XM_017022184.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X9	XM_017022185.2:c.1374+102=	XM_017022185.2:c.1374+101_1374+102insCT	XM_017022185.2:c.1374+101_1374+102insCTT	XM_017022185.2:c.1374+101_1374+102insCTTTT	XM_017022185.2:c.1374+101_1374+102insCTTTTT	XM_017022185.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X3	XM_024449920.2:c.1374+102=	XM_024449920.2:c.1374+101_1374+102insCT	XM_024449920.2:c.1374+101_1374+102insCTT	XM_024449920.2:c.1374+101_1374+102insCTTTT	XM_024449920.2:c.1374+101_1374+102insCTTTTT	XM_024449920.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X1	XM_024449921.2:c.1374+102=	XM_024449921.2:c.1374+101_1374+102insCT	XM_024449921.2:c.1374+101_1374+102insCTT	XM_024449921.2:c.1374+101_1374+102insCTTTT	XM_024449921.2:c.1374+101_1374+102insCTTTTT	XM_024449921.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X7	XM_024449922.2:c.1374+102=	XM_024449922.2:c.1374+101_1374+102insCT	XM_024449922.2:c.1374+101_1374+102insCTT	XM_024449922.2:c.1374+101_1374+102insCTTTT	XM_024449922.2:c.1374+101_1374+102insCTTTTT	XM_024449922.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X6	XM_024449923.2:c.1374+102=	XM_024449923.2:c.1374+101_1374+102insCT	XM_024449923.2:c.1374+101_1374+102insCTT	XM_024449923.2:c.1374+101_1374+102insCTTTT	XM_024449923.2:c.1374+101_1374+102insCTTTTT	XM_024449923.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X8	XM_024449924.2:c.1374+102=	XM_024449924.2:c.1374+101_1374+102insCT	XM_024449924.2:c.1374+101_1374+102insCTT	XM_024449924.2:c.1374+101_1374+102insCTTTT	XM_024449924.2:c.1374+101_1374+102insCTTTTT	XM_024449924.2:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X4	XM_047432507.1:c.1374+102=	XM_047432507.1:c.1374+101_1374+102insCT	XM_047432507.1:c.1374+101_1374+102insCTT	XM_047432507.1:c.1374+101_1374+102insCTTTT	XM_047432507.1:c.1374+101_1374+102insCTTTTT	XM_047432507.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X10	XM_047432508.1:c.1374+102=	XM_047432508.1:c.1374+101_1374+102insCT	XM_047432508.1:c.1374+101_1374+102insCTT	XM_047432508.1:c.1374+101_1374+102insCTTTT	XM_047432508.1:c.1374+101_1374+102insCTTTTT	XM_047432508.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X11	XM_047432509.1:c.1374+102=	XM_047432509.1:c.1374+101_1374+102insCT	XM_047432509.1:c.1374+101_1374+102insCTT	XM_047432509.1:c.1374+101_1374+102insCTTTT	XM_047432509.1:c.1374+101_1374+102insCTTTTT	XM_047432509.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X12	XM_047432510.1:c.1374+102=	XM_047432510.1:c.1374+101_1374+102insCT	XM_047432510.1:c.1374+101_1374+102insCTT	XM_047432510.1:c.1374+101_1374+102insCTTTT	XM_047432510.1:c.1374+101_1374+102insCTTTTT	XM_047432510.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X13	XM_047432511.1:c.1374+102=	XM_047432511.1:c.1374+101_1374+102insCT	XM_047432511.1:c.1374+101_1374+102insCTT	XM_047432511.1:c.1374+101_1374+102insCTTTT	XM_047432511.1:c.1374+101_1374+102insCTTTTT	XM_047432511.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X14	XM_047432512.1:c.1374+102=	XM_047432512.1:c.1374+101_1374+102insCT	XM_047432512.1:c.1374+101_1374+102insCTT	XM_047432512.1:c.1374+101_1374+102insCTTTT	XM_047432512.1:c.1374+101_1374+102insCTTTTT	XM_047432512.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X15	XM_047432513.1:c.1374+102=	XM_047432513.1:c.1374+101_1374+102insCT	XM_047432513.1:c.1374+101_1374+102insCTT	XM_047432513.1:c.1374+101_1374+102insCTTTT	XM_047432513.1:c.1374+101_1374+102insCTTTTT	XM_047432513.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X16	XM_047432514.1:c.1374+102=	XM_047432514.1:c.1374+101_1374+102insCT	XM_047432514.1:c.1374+101_1374+102insCTT	XM_047432514.1:c.1374+101_1374+102insCTTTT	XM_047432514.1:c.1374+101_1374+102insCTTTTT	XM_047432514.1:c.1374+101_1374+102insCTTTTTT
MAN2A2 transcript variant X17	XM_047432515.1:c.314+102=	XM_047432515.1:c.314+101_314+102insCT	XM_047432515.1:c.314+101_314+102insCTT	XM_047432515.1:c.314+101_314+102insCTTTT	XM_047432515.1:c.314+101_314+102insCTTTTT	XM_047432515.1:c.314+101_314+102insCTTTTTT
MAN2A2 transcript variant X18	XM_047432516.1:c.314+102=	XM_047432516.1:c.314+101_314+102insCT	XM_047432516.1:c.314+101_314+102insCTT	XM_047432516.1:c.314+101_314+102insCTTTT	XM_047432516.1:c.314+101_314+102insCTTTTT	XM_047432516.1:c.314+101_314+102insCTTTTTT

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#.

8 SubSNP, 8 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	EVA_DECODE	ss3698449459	Jul 13, 2019 (153)
2	ACPOP	ss3741164522	Jul 13, 2019 (153)
3	GNOMAD	ss4293715225	Apr 26, 2021 (155)
4	GNOMAD	ss4293715226	Apr 26, 2021 (155)
5	GNOMAD	ss4293715227	Apr 26, 2021 (155)
6	GNOMAD	ss4293715228	Apr 26, 2021 (155)
7	GNOMAD	ss4293715229	Apr 26, 2021 (155)
8	TOMMO_GENOMICS	ss5771732085	Oct 17, 2022 (156)
9	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477336032 (NC_000015.10:90909605::CT 149/131850) Row 477336033 (NC_000015.10:90909605::CTT 3/131858) Row 477336034 (NC_000015.10:90909605::CTTTT 1/131860)...	-	Apr 26, 2021 (155)
10	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477336032 (NC_000015.10:90909605::CT 149/131850) Row 477336033 (NC_000015.10:90909605::CTT 3/131858) Row 477336034 (NC_000015.10:90909605::CTTTT 1/131860)...	-	Apr 26, 2021 (155)
11	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477336032 (NC_000015.10:90909605::CT 149/131850) Row 477336033 (NC_000015.10:90909605::CTT 3/131858) Row 477336034 (NC_000015.10:90909605::CTTTT 1/131860)...	-	Apr 26, 2021 (155)
12	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477336032 (NC_000015.10:90909605::CT 149/131850) Row 477336033 (NC_000015.10:90909605::CTT 3/131858) Row 477336034 (NC_000015.10:90909605::CTTTT 1/131860)...	-	Apr 26, 2021 (155)
13	gnomAD - Genomes Submission ignored due to conflicting rows: Row 477336032 (NC_000015.10:90909605::CT 149/131850) Row 477336033 (NC_000015.10:90909605::CTT 3/131858) Row 477336034 (NC_000015.10:90909605::CTTTT 1/131860)...	-	Apr 26, 2021 (155)
14	Northern Sweden	NC_000015.9 - 91452836	Jul 13, 2019 (153)
15	14KJPN	NC_000015.10 - 90909606	Oct 17, 2022 (156)
16	ALFA	NC_000015.10 - 90909606	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
14449387, ss3741164522	NC_000015.9:91452835::CT	NC_000015.10:90909605::CT	(self)
105569189, 12070521707, ss3698449459, ss4293715225, ss5771732085	NC_000015.10:90909605::CT	NC_000015.10:90909605::CT	(self)
12070521707, ss4293715226	NC_000015.10:90909605::CTT	NC_000015.10:90909605::CTT	(self)
12070521707, ss4293715227	NC_000015.10:90909605::CTTTT	NC_000015.10:90909605::CTTTT	(self)
12070521707, ss4293715228	NC_000015.10:90909605::CTTTTT	NC_000015.10:90909605::CTTTTT	(self)
ss4293715229	NC_000015.10:90909605::CTTTTTT	NC_000015.10:90909605::CTTTTTT	(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 rs1491374744

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

rs1491374744