Name: rs1554343030
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.

rs1554343030

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:36412328-36412345 (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)₈ / del(T)₇ / del(T)₆ / del(…
del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₆
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₈=0.0000 (0/7786, ALFA)
del(T)₇=0.0000 (0/7786, ALFA)
del(T)₆=0.0000 (0/7786, ALFA) (+ 8 more)
del(T)₅=0.0000 (0/7786, ALFA)
del(T)₄=0.0000 (0/7786, ALFA)
delTTT=0.0000 (0/7786, ALFA)
delTT=0.0000 (0/7786, ALFA)
delT=0.0000 (0/7786, ALFA)
dupT=0.0000 (0/7786, ALFA)
dupTT=0.0000 (0/7786, ALFA)
dup(T)₄=0.0000 (0/7786, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ANLN : 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	7786	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	5076	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	1688	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	64	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	1624	TTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	90	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	72	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	18	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	98	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	450	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	72	TTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	312	TTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=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").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	7786	(T)₁₈=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	European	Sub	5076	(T)₁₈=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	African	Sub	1688	(T)₁₈=1.0000	del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dup(T)₄=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	450	(T)₁₈=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Other	Sub	312	(T)₁₈=1.000	del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dup(T)₄=0.000
Allele Frequency Aggregator	Latin American 1	Sub	98	(T)₁₈=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	Asian	Sub	90	(T)₁₈=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=0.00
Allele Frequency Aggregator	South Asian	Sub	72	(T)₁₈=1.00	del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dup(T)₄=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 7	NC_000007.14:g.36412338_36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412339_36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412340_36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412341_36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412342_36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412343_36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412344_36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412345del
GRCh38.p14 chr 7	NC_000007.14:g.36412345dup
GRCh38.p14 chr 7	NC_000007.14:g.36412344_36412345dup
GRCh38.p14 chr 7	NC_000007.14:g.36412343_36412345dup
GRCh38.p14 chr 7	NC_000007.14:g.36412342_36412345dup
GRCh38.p14 chr 7	NC_000007.14:g.36412340_36412345dup
GRCh37.p13 chr 7	NC_000007.13:g.36451947_36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451948_36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451949_36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451950_36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451951_36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451952_36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451953_36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451954del
GRCh37.p13 chr 7	NC_000007.13:g.36451954dup
GRCh37.p13 chr 7	NC_000007.13:g.36451953_36451954dup
GRCh37.p13 chr 7	NC_000007.13:g.36451952_36451954dup
GRCh37.p13 chr 7	NC_000007.13:g.36451951_36451954dup
GRCh37.p13 chr 7	NC_000007.13:g.36451949_36451954dup
ANLN RefSeqGene	NG_041770.1:g.27536_27543del
ANLN RefSeqGene	NG_041770.1:g.27537_27543del
ANLN RefSeqGene	NG_041770.1:g.27538_27543del
ANLN RefSeqGene	NG_041770.1:g.27539_27543del
ANLN RefSeqGene	NG_041770.1:g.27540_27543del
ANLN RefSeqGene	NG_041770.1:g.27541_27543del
ANLN RefSeqGene	NG_041770.1:g.27542_27543del
ANLN RefSeqGene	NG_041770.1:g.27543del
ANLN RefSeqGene	NG_041770.1:g.27543dup
ANLN RefSeqGene	NG_041770.1:g.27542_27543dup
ANLN RefSeqGene	NG_041770.1:g.27541_27543dup
ANLN RefSeqGene	NG_041770.1:g.27540_27543dup
ANLN RefSeqGene	NG_041770.1:g.27538_27543dup

Gene: ANLN, anillin actin binding protein (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ANLN transcript variant 2	NM_001284301.3:c.1395+117… NM_001284301.3:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant 3	NM_001284302.3:c.1395+117… NM_001284302.3:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant 1	NM_018685.5:c.1395+1172_1… NM_018685.5:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant X1	XM_006715746.3:c.1395+117… XM_006715746.3:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant X4	XM_006715747.5:c.1395+117… XM_006715747.5:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant X2	XM_017012354.3:c.1395+117… XM_017012354.3:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant X3	XM_017012355.3:c.1395+117… XM_017012355.3:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant X6	XM_017012356.3:c.1395+117… XM_017012356.3:c.1395+1172_1395+1179del	N/A	Intron Variant
ANLN transcript variant X5	XM_047420504.1:c.1395+117… XM_047420504.1:c.1395+1172_1395+1179del	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)₁₈=	del(T)₈	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₆
GRCh38.p14 chr 7	NC_000007.14:g.36412328_36412345=	NC_000007.14:g.36412338_36412345del	NC_000007.14:g.36412339_36412345del	NC_000007.14:g.36412340_36412345del	NC_000007.14:g.36412341_36412345del	NC_000007.14:g.36412342_36412345del	NC_000007.14:g.36412343_36412345del	NC_000007.14:g.36412344_36412345del	NC_000007.14:g.36412345del	NC_000007.14:g.36412345dup	NC_000007.14:g.36412344_36412345dup	NC_000007.14:g.36412343_36412345dup	NC_000007.14:g.36412342_36412345dup	NC_000007.14:g.36412340_36412345dup
GRCh37.p13 chr 7	NC_000007.13:g.36451937_36451954=	NC_000007.13:g.36451947_36451954del	NC_000007.13:g.36451948_36451954del	NC_000007.13:g.36451949_36451954del	NC_000007.13:g.36451950_36451954del	NC_000007.13:g.36451951_36451954del	NC_000007.13:g.36451952_36451954del	NC_000007.13:g.36451953_36451954del	NC_000007.13:g.36451954del	NC_000007.13:g.36451954dup	NC_000007.13:g.36451953_36451954dup	NC_000007.13:g.36451952_36451954dup	NC_000007.13:g.36451951_36451954dup	NC_000007.13:g.36451949_36451954dup
ANLN RefSeqGene	NG_041770.1:g.27526_27543=	NG_041770.1:g.27536_27543del	NG_041770.1:g.27537_27543del	NG_041770.1:g.27538_27543del	NG_041770.1:g.27539_27543del	NG_041770.1:g.27540_27543del	NG_041770.1:g.27541_27543del	NG_041770.1:g.27542_27543del	NG_041770.1:g.27543del	NG_041770.1:g.27543dup	NG_041770.1:g.27542_27543dup	NG_041770.1:g.27541_27543dup	NG_041770.1:g.27540_27543dup	NG_041770.1:g.27538_27543dup
ANLN transcript variant 2	NM_001284301.3:c.1395+1162=	NM_001284301.3:c.1395+1172_1395+1179del	NM_001284301.3:c.1395+1173_1395+1179del	NM_001284301.3:c.1395+1174_1395+1179del	NM_001284301.3:c.1395+1175_1395+1179del	NM_001284301.3:c.1395+1176_1395+1179del	NM_001284301.3:c.1395+1177_1395+1179del	NM_001284301.3:c.1395+1178_1395+1179del	NM_001284301.3:c.1395+1179del	NM_001284301.3:c.1395+1179dup	NM_001284301.3:c.1395+1178_1395+1179dup	NM_001284301.3:c.1395+1177_1395+1179dup	NM_001284301.3:c.1395+1176_1395+1179dup	NM_001284301.3:c.1395+1174_1395+1179dup
ANLN transcript variant 3	NM_001284302.3:c.1395+1162=	NM_001284302.3:c.1395+1172_1395+1179del	NM_001284302.3:c.1395+1173_1395+1179del	NM_001284302.3:c.1395+1174_1395+1179del	NM_001284302.3:c.1395+1175_1395+1179del	NM_001284302.3:c.1395+1176_1395+1179del	NM_001284302.3:c.1395+1177_1395+1179del	NM_001284302.3:c.1395+1178_1395+1179del	NM_001284302.3:c.1395+1179del	NM_001284302.3:c.1395+1179dup	NM_001284302.3:c.1395+1178_1395+1179dup	NM_001284302.3:c.1395+1177_1395+1179dup	NM_001284302.3:c.1395+1176_1395+1179dup	NM_001284302.3:c.1395+1174_1395+1179dup
ANLN transcript	NM_018685.2:c.1395+1162=	NM_018685.2:c.1395+1172_1395+1179del	NM_018685.2:c.1395+1173_1395+1179del	NM_018685.2:c.1395+1174_1395+1179del	NM_018685.2:c.1395+1175_1395+1179del	NM_018685.2:c.1395+1176_1395+1179del	NM_018685.2:c.1395+1177_1395+1179del	NM_018685.2:c.1395+1178_1395+1179del	NM_018685.2:c.1395+1179del	NM_018685.2:c.1395+1179dup	NM_018685.2:c.1395+1178_1395+1179dup	NM_018685.2:c.1395+1177_1395+1179dup	NM_018685.2:c.1395+1176_1395+1179dup	NM_018685.2:c.1395+1174_1395+1179dup
ANLN transcript variant 1	NM_018685.5:c.1395+1162=	NM_018685.5:c.1395+1172_1395+1179del	NM_018685.5:c.1395+1173_1395+1179del	NM_018685.5:c.1395+1174_1395+1179del	NM_018685.5:c.1395+1175_1395+1179del	NM_018685.5:c.1395+1176_1395+1179del	NM_018685.5:c.1395+1177_1395+1179del	NM_018685.5:c.1395+1178_1395+1179del	NM_018685.5:c.1395+1179del	NM_018685.5:c.1395+1179dup	NM_018685.5:c.1395+1178_1395+1179dup	NM_018685.5:c.1395+1177_1395+1179dup	NM_018685.5:c.1395+1176_1395+1179dup	NM_018685.5:c.1395+1174_1395+1179dup
ANLN transcript variant X1	XM_005249777.1:c.1395+1162=	XM_005249777.1:c.1395+1172_1395+1179del	XM_005249777.1:c.1395+1173_1395+1179del	XM_005249777.1:c.1395+1174_1395+1179del	XM_005249777.1:c.1395+1175_1395+1179del	XM_005249777.1:c.1395+1176_1395+1179del	XM_005249777.1:c.1395+1177_1395+1179del	XM_005249777.1:c.1395+1178_1395+1179del	XM_005249777.1:c.1395+1179del	XM_005249777.1:c.1395+1179dup	XM_005249777.1:c.1395+1178_1395+1179dup	XM_005249777.1:c.1395+1177_1395+1179dup	XM_005249777.1:c.1395+1176_1395+1179dup	XM_005249777.1:c.1395+1174_1395+1179dup
ANLN transcript variant X2	XM_005249778.1:c.1395+1162=	XM_005249778.1:c.1395+1172_1395+1179del	XM_005249778.1:c.1395+1173_1395+1179del	XM_005249778.1:c.1395+1174_1395+1179del	XM_005249778.1:c.1395+1175_1395+1179del	XM_005249778.1:c.1395+1176_1395+1179del	XM_005249778.1:c.1395+1177_1395+1179del	XM_005249778.1:c.1395+1178_1395+1179del	XM_005249778.1:c.1395+1179del	XM_005249778.1:c.1395+1179dup	XM_005249778.1:c.1395+1178_1395+1179dup	XM_005249778.1:c.1395+1177_1395+1179dup	XM_005249778.1:c.1395+1176_1395+1179dup	XM_005249778.1:c.1395+1174_1395+1179dup
ANLN transcript variant X3	XM_005249779.1:c.-145+1162=	XM_005249779.1:c.-145+1172_-145+1179del	XM_005249779.1:c.-145+1173_-145+1179del	XM_005249779.1:c.-145+1174_-145+1179del	XM_005249779.1:c.-145+1175_-145+1179del	XM_005249779.1:c.-145+1176_-145+1179del	XM_005249779.1:c.-145+1177_-145+1179del	XM_005249779.1:c.-145+1178_-145+1179del	XM_005249779.1:c.-145+1179del	XM_005249779.1:c.-145+1179dup	XM_005249779.1:c.-145+1178_-145+1179dup	XM_005249779.1:c.-145+1177_-145+1179dup	XM_005249779.1:c.-145+1176_-145+1179dup	XM_005249779.1:c.-145+1174_-145+1179dup
ANLN transcript variant X1	XM_006715746.3:c.1395+1162=	XM_006715746.3:c.1395+1172_1395+1179del	XM_006715746.3:c.1395+1173_1395+1179del	XM_006715746.3:c.1395+1174_1395+1179del	XM_006715746.3:c.1395+1175_1395+1179del	XM_006715746.3:c.1395+1176_1395+1179del	XM_006715746.3:c.1395+1177_1395+1179del	XM_006715746.3:c.1395+1178_1395+1179del	XM_006715746.3:c.1395+1179del	XM_006715746.3:c.1395+1179dup	XM_006715746.3:c.1395+1178_1395+1179dup	XM_006715746.3:c.1395+1177_1395+1179dup	XM_006715746.3:c.1395+1176_1395+1179dup	XM_006715746.3:c.1395+1174_1395+1179dup
ANLN transcript variant X4	XM_006715747.5:c.1395+1162=	XM_006715747.5:c.1395+1172_1395+1179del	XM_006715747.5:c.1395+1173_1395+1179del	XM_006715747.5:c.1395+1174_1395+1179del	XM_006715747.5:c.1395+1175_1395+1179del	XM_006715747.5:c.1395+1176_1395+1179del	XM_006715747.5:c.1395+1177_1395+1179del	XM_006715747.5:c.1395+1178_1395+1179del	XM_006715747.5:c.1395+1179del	XM_006715747.5:c.1395+1179dup	XM_006715747.5:c.1395+1178_1395+1179dup	XM_006715747.5:c.1395+1177_1395+1179dup	XM_006715747.5:c.1395+1176_1395+1179dup	XM_006715747.5:c.1395+1174_1395+1179dup
ANLN transcript variant X2	XM_017012354.3:c.1395+1162=	XM_017012354.3:c.1395+1172_1395+1179del	XM_017012354.3:c.1395+1173_1395+1179del	XM_017012354.3:c.1395+1174_1395+1179del	XM_017012354.3:c.1395+1175_1395+1179del	XM_017012354.3:c.1395+1176_1395+1179del	XM_017012354.3:c.1395+1177_1395+1179del	XM_017012354.3:c.1395+1178_1395+1179del	XM_017012354.3:c.1395+1179del	XM_017012354.3:c.1395+1179dup	XM_017012354.3:c.1395+1178_1395+1179dup	XM_017012354.3:c.1395+1177_1395+1179dup	XM_017012354.3:c.1395+1176_1395+1179dup	XM_017012354.3:c.1395+1174_1395+1179dup
ANLN transcript variant X3	XM_017012355.3:c.1395+1162=	XM_017012355.3:c.1395+1172_1395+1179del	XM_017012355.3:c.1395+1173_1395+1179del	XM_017012355.3:c.1395+1174_1395+1179del	XM_017012355.3:c.1395+1175_1395+1179del	XM_017012355.3:c.1395+1176_1395+1179del	XM_017012355.3:c.1395+1177_1395+1179del	XM_017012355.3:c.1395+1178_1395+1179del	XM_017012355.3:c.1395+1179del	XM_017012355.3:c.1395+1179dup	XM_017012355.3:c.1395+1178_1395+1179dup	XM_017012355.3:c.1395+1177_1395+1179dup	XM_017012355.3:c.1395+1176_1395+1179dup	XM_017012355.3:c.1395+1174_1395+1179dup
ANLN transcript variant X6	XM_017012356.3:c.1395+1162=	XM_017012356.3:c.1395+1172_1395+1179del	XM_017012356.3:c.1395+1173_1395+1179del	XM_017012356.3:c.1395+1174_1395+1179del	XM_017012356.3:c.1395+1175_1395+1179del	XM_017012356.3:c.1395+1176_1395+1179del	XM_017012356.3:c.1395+1177_1395+1179del	XM_017012356.3:c.1395+1178_1395+1179del	XM_017012356.3:c.1395+1179del	XM_017012356.3:c.1395+1179dup	XM_017012356.3:c.1395+1178_1395+1179dup	XM_017012356.3:c.1395+1177_1395+1179dup	XM_017012356.3:c.1395+1176_1395+1179dup	XM_017012356.3:c.1395+1174_1395+1179dup
ANLN transcript variant X5	XM_047420504.1:c.1395+1162=	XM_047420504.1:c.1395+1172_1395+1179del	XM_047420504.1:c.1395+1173_1395+1179del	XM_047420504.1:c.1395+1174_1395+1179del	XM_047420504.1:c.1395+1175_1395+1179del	XM_047420504.1:c.1395+1176_1395+1179del	XM_047420504.1:c.1395+1177_1395+1179del	XM_047420504.1:c.1395+1178_1395+1179del	XM_047420504.1:c.1395+1179del	XM_047420504.1:c.1395+1179dup	XM_047420504.1:c.1395+1178_1395+1179dup	XM_047420504.1:c.1395+1177_1395+1179dup	XM_047420504.1:c.1395+1176_1395+1179dup	XM_047420504.1:c.1395+1174_1395+1179dup

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#.

28 SubSNP, 22 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HUMANGENOME_JCVI	ss95969347	Feb 06, 2009 (130)
2	ACPOP	ss3734526989	Jul 13, 2019 (153)
3	ACPOP	ss3734526990	Jul 13, 2019 (153)
4	ACPOP	ss3734526991	Jul 13, 2019 (153)
5	KOGIC	ss3961238871	Apr 26, 2020 (154)
6	KOGIC	ss3961238872	Apr 26, 2020 (154)
7	GNOMAD	ss4161502392	Apr 26, 2021 (155)
8	GNOMAD	ss4161502407	Apr 26, 2021 (155)
9	GNOMAD	ss4161502408	Apr 26, 2021 (155)
10	GNOMAD	ss4161502409	Apr 26, 2021 (155)
11	GNOMAD	ss4161502410	Apr 26, 2021 (155)
12	GNOMAD	ss4161502411	Apr 26, 2021 (155)
13	GNOMAD	ss4161502412	Apr 26, 2021 (155)
14	GNOMAD	ss4161502413	Apr 26, 2021 (155)
15	GNOMAD	ss4161502414	Apr 26, 2021 (155)
16	GNOMAD	ss4161502415	Apr 26, 2021 (155)
17	GNOMAD	ss4161502416	Apr 26, 2021 (155)
18	TOMMO_GENOMICS	ss5182635008	Apr 26, 2021 (155)
19	TOMMO_GENOMICS	ss5182635010	Apr 26, 2021 (155)
20	TOMMO_GENOMICS	ss5182635011	Apr 26, 2021 (155)
21	1000G_HIGH_COVERAGE	ss5272475770	Oct 13, 2022 (156)
22	HUGCELL_USP	ss5469692178	Oct 13, 2022 (156)
23	HUGCELL_USP	ss5469692179	Oct 13, 2022 (156)
24	HUGCELL_USP	ss5469692180	Oct 13, 2022 (156)
25	HUGCELL_USP	ss5469692181	Oct 13, 2022 (156)
26	SANFORD_IMAGENETICS	ss5642718349	Oct 13, 2022 (156)
27	TOMMO_GENOMICS	ss5722321385	Oct 13, 2022 (156)
28	TOMMO_GENOMICS	ss5722321386	Oct 13, 2022 (156)
29	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
30	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 258206474 (NC_000007.14:36412327::T 1219/87392) Row 258206489 (NC_000007.14:36412327::TT 45/87394) Row 258206490 (NC_000007.14:36412327::TTT 1/87406)...	-	Apr 26, 2021 (155)
40	Korean Genome Project Submission ignored due to conflicting rows: Row 17616872 (NC_000007.14:36412327:TT: 99/1710) Row 17616873 (NC_000007.14:36412328:T: 50/1710)	-	Apr 26, 2020 (154)
41	Korean Genome Project Submission ignored due to conflicting rows: Row 17616872 (NC_000007.14:36412327:TT: 99/1710) Row 17616873 (NC_000007.14:36412328:T: 50/1710)	-	Apr 26, 2020 (154)
42	Northern Sweden Submission ignored due to conflicting rows: Row 7811854 (NC_000007.13:36451936:T: 30/536) Row 7811855 (NC_000007.13:36451936:TT: 10/536) Row 7811856 (NC_000007.13:36451936:TTT: 8/536)	-	Jul 13, 2019 (153)
43	Northern Sweden Submission ignored due to conflicting rows: Row 7811854 (NC_000007.13:36451936:T: 30/536) Row 7811855 (NC_000007.13:36451936:TT: 10/536) Row 7811856 (NC_000007.13:36451936:TTT: 8/536)	-	Jul 13, 2019 (153)
44	Northern Sweden Submission ignored due to conflicting rows: Row 7811854 (NC_000007.13:36451936:T: 30/536) Row 7811855 (NC_000007.13:36451936:TT: 10/536) Row 7811856 (NC_000007.13:36451936:TTT: 8/536)	-	Jul 13, 2019 (153)
45	8.3KJPN Submission ignored due to conflicting rows: Row 40604315 (NC_000007.13:36451936:TT: 506/16002) Row 40604317 (NC_000007.13:36451936:T: 112/16002) Row 40604318 (NC_000007.13:36451936:TTT: 46/16002)	-	Apr 26, 2021 (155)
46	8.3KJPN Submission ignored due to conflicting rows: Row 40604315 (NC_000007.13:36451936:TT: 506/16002) Row 40604317 (NC_000007.13:36451936:T: 112/16002) Row 40604318 (NC_000007.13:36451936:TTT: 46/16002)	-	Apr 26, 2021 (155)
47	8.3KJPN Submission ignored due to conflicting rows: Row 40604315 (NC_000007.13:36451936:TT: 506/16002) Row 40604317 (NC_000007.13:36451936:T: 112/16002) Row 40604318 (NC_000007.13:36451936:TTT: 46/16002)	-	Apr 26, 2021 (155)
48	14KJPN Submission ignored due to conflicting rows: Row 56158489 (NC_000007.14:36412327:T: 233/27704) Row 56158490 (NC_000007.14:36412327:TT: 893/27704)	-	Oct 13, 2022 (156)
49	14KJPN Submission ignored due to conflicting rows: Row 56158489 (NC_000007.14:36412327:T: 233/27704) Row 56158490 (NC_000007.14:36412327:TT: 893/27704)	-	Oct 13, 2022 (156)
50	ALFA	NC_000007.14 - 36412328	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
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4161502416	NC_000007.14:36412327:TTTTTT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4161502415	NC_000007.14:36412327:TTTTT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4161502414	NC_000007.14:36412327:TTTT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3734526991, ss5182635011	NC_000007.13:36451936:TTT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4161502413, ss5272475770, ss5469692180	NC_000007.14:36412327:TTT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3734526990, ss5182635008, ss5642718349	NC_000007.13:36451936:TT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3961238871, ss4161502412, ss5469692178, ss5722321386	NC_000007.14:36412327:TT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss3734526989, ss5182635010	NC_000007.13:36451936:T:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4161502411, ss5469692179, ss5722321385	NC_000007.14:36412327:T:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3961238872	NC_000007.14:36412328:T:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4161502392, ss5469692181	NC_000007.14:36412327::T	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss95969347	NT_007819.17:36441937::T	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4161502407	NC_000007.14:36412327::TT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4161502408	NC_000007.14:36412327::TTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4161502409	NC_000007.14:36412327::TTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7696963219	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4161502410	NC_000007.14:36412327::TTTTTT	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3527278660	NC_000007.14:36412327:TTTTTTT:	NC_000007.14:36412327:TTTTTTTTTTTT… NC_000007.14:36412327:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

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

No publications for rs1554343030

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

rs1554343030