Name: rs141874345
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.

rs141874345

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr14:69102108-69102126 (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)₇ / del(T)₆ / del(T)₅ / del(…
del(T)₇ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₇
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.1094 (998/9124, ALFA)
delT=0.1400 (701/5008, 1000G)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: DCAF5 : 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	9124	TTTTTTTTTTTTTTTTTTT=0.8900	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1094, TTTTTTTTTTTTTTTTTTTTT=0.0007	0.826602	0.045215	0.128183	32
European	Sub	7284	TTTTTTTTTTTTTTTTTTT=0.8626	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.1366, TTTTTTTTTTTTTTTTTTTTT=0.0008	0.783278	0.056381	0.160341	32
African	Sub	1064	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
African Others	Sub	52	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	1012	TTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	0.0	0.0	N/A
Asian	Sub	94	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	74	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	20	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	64	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	340	TTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	72	TTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	206	TTTTTTTTTTTTTTTTTTT=0.985	TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.015, TTTTTTTTTTTTTTTTTTTTT=0.000	0.980583	0.009709	0.009709	24

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	9124	(T)₁₉=0.8900	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1094, dupTT=0.0007
Allele Frequency Aggregator	European	Sub	7284	(T)₁₉=0.8626	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.1366, dupTT=0.0008
Allele Frequency Aggregator	African	Sub	1064	(T)₁₉=1.0000	del(T)₇=0.0000, del(T)₆=0.0000, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	340	(T)₁₉=1.000	del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000
Allele Frequency Aggregator	Other	Sub	206	(T)₁₉=0.985	del(T)₇=0.000, del(T)₆=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.015, dupTT=0.000
Allele Frequency Aggregator	Asian	Sub	94	(T)₁₉=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	South Asian	Sub	72	(T)₁₉=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
Allele Frequency Aggregator	Latin American 1	Sub	64	(T)₁₉=1.00	del(T)₇=0.00, del(T)₆=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00
1000Genomes	Global	Study-wide	5008	(T)₁₉=0.8600	delT=0.1400
1000Genomes	African	Sub	1322	(T)₁₉=0.8865	delT=0.1135
1000Genomes	East Asian	Sub	1008	(T)₁₉=0.8929	delT=0.1071
1000Genomes	Europe	Sub	1006	(T)₁₉=0.8598	delT=0.1402
1000Genomes	South Asian	Sub	978	(T)₁₉=0.865	delT=0.135
1000Genomes	American	Sub	694	(T)₁₉=0.755	delT=0.245

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

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 14	NC_000014.9:g.69102120_69102126del
GRCh38.p14 chr 14	NC_000014.9:g.69102121_69102126del
GRCh38.p14 chr 14	NC_000014.9:g.69102122_69102126del
GRCh38.p14 chr 14	NC_000014.9:g.69102123_69102126del
GRCh38.p14 chr 14	NC_000014.9:g.69102124_69102126del
GRCh38.p14 chr 14	NC_000014.9:g.69102125_69102126del
GRCh38.p14 chr 14	NC_000014.9:g.69102126del
GRCh38.p14 chr 14	NC_000014.9:g.69102126dup
GRCh38.p14 chr 14	NC_000014.9:g.69102125_69102126dup
GRCh38.p14 chr 14	NC_000014.9:g.69102124_69102126dup
GRCh38.p14 chr 14	NC_000014.9:g.69102123_69102126dup
GRCh38.p14 chr 14	NC_000014.9:g.69102122_69102126dup
GRCh38.p14 chr 14	NC_000014.9:g.69102120_69102126dup
GRCh37.p13 chr 14	NC_000014.8:g.69568837_69568843del
GRCh37.p13 chr 14	NC_000014.8:g.69568838_69568843del
GRCh37.p13 chr 14	NC_000014.8:g.69568839_69568843del
GRCh37.p13 chr 14	NC_000014.8:g.69568840_69568843del
GRCh37.p13 chr 14	NC_000014.8:g.69568841_69568843del
GRCh37.p13 chr 14	NC_000014.8:g.69568842_69568843del
GRCh37.p13 chr 14	NC_000014.8:g.69568843del
GRCh37.p13 chr 14	NC_000014.8:g.69568843dup
GRCh37.p13 chr 14	NC_000014.8:g.69568842_69568843dup
GRCh37.p13 chr 14	NC_000014.8:g.69568841_69568843dup
GRCh37.p13 chr 14	NC_000014.8:g.69568840_69568843dup
GRCh37.p13 chr 14	NC_000014.8:g.69568839_69568843dup
GRCh37.p13 chr 14	NC_000014.8:g.69568837_69568843dup

Gene: DCAF5, DDB1 and CUL4 associated factor 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
DCAF5 transcript variant 2	NM_001284206.1:c.663-1022… NM_001284206.1:c.663-10227_663-10221del	N/A	Intron Variant
DCAF5 transcript variant 3	NM_001284207.1:c.420-1022… NM_001284207.1:c.420-10227_420-10221del	N/A	Intron Variant
DCAF5 transcript variant 4	NM_001284208.2:c.666-1022… NM_001284208.2:c.666-10227_666-10221del	N/A	Intron Variant
DCAF5 transcript variant 1	NM_003861.3:c.666-10227_6… NM_003861.3:c.666-10227_666-10221del	N/A	Intron Variant
DCAF5 transcript variant X1	XM_006720297.3:c.666-1022… XM_006720297.3:c.666-10227_666-10221del	N/A	Intron Variant
DCAF5 transcript variant X2	XM_006720298.3:c.663-1022… XM_006720298.3:c.663-10227_663-10221del	N/A	Intron Variant
DCAF5 transcript variant X3	XM_006720299.4:c.420-1022… XM_006720299.4:c.420-10227_420-10221del	N/A	Intron Variant
DCAF5 transcript variant X7	XM_011537278.2:c.420-1022… XM_011537278.2:c.420-10227_420-10221del	N/A	Intron Variant
DCAF5 transcript variant X4	XM_011537279.3:c.420-1022… XM_011537279.3:c.420-10227_420-10221del	N/A	Intron Variant
DCAF5 transcript variant X9	XM_011537280.4:c.15-10227… XM_011537280.4:c.15-10227_15-10221del	N/A	Intron Variant
DCAF5 transcript variant X5	XM_017021733.2:c.420-1022… XM_017021733.2:c.420-10227_420-10221del	N/A	Intron Variant
DCAF5 transcript variant X10	XM_017021737.2:c.15-10227… XM_017021737.2:c.15-10227_15-10221del	N/A	Intron Variant
DCAF5 transcript variant X6	XM_047431846.1:c.420-1022… XM_047431846.1:c.420-10227_420-10221del	N/A	Intron Variant
DCAF5 transcript variant X8	XM_047431847.1:c.420-1022… XM_047431847.1:c.420-10227_420-10221del	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)₁₉=	del(T)₇	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₇
GRCh38.p14 chr 14	NC_000014.9:g.69102108_69102126=	NC_000014.9:g.69102120_69102126del	NC_000014.9:g.69102121_69102126del	NC_000014.9:g.69102122_69102126del	NC_000014.9:g.69102123_69102126del	NC_000014.9:g.69102124_69102126del	NC_000014.9:g.69102125_69102126del	NC_000014.9:g.69102126del	NC_000014.9:g.69102126dup	NC_000014.9:g.69102125_69102126dup	NC_000014.9:g.69102124_69102126dup	NC_000014.9:g.69102123_69102126dup	NC_000014.9:g.69102122_69102126dup	NC_000014.9:g.69102120_69102126dup
GRCh37.p13 chr 14	NC_000014.8:g.69568825_69568843=	NC_000014.8:g.69568837_69568843del	NC_000014.8:g.69568838_69568843del	NC_000014.8:g.69568839_69568843del	NC_000014.8:g.69568840_69568843del	NC_000014.8:g.69568841_69568843del	NC_000014.8:g.69568842_69568843del	NC_000014.8:g.69568843del	NC_000014.8:g.69568843dup	NC_000014.8:g.69568842_69568843dup	NC_000014.8:g.69568841_69568843dup	NC_000014.8:g.69568840_69568843dup	NC_000014.8:g.69568839_69568843dup	NC_000014.8:g.69568837_69568843dup
DCAF5 transcript variant 2	NM_001284206.1:c.663-10221=	NM_001284206.1:c.663-10227_663-10221del	NM_001284206.1:c.663-10226_663-10221del	NM_001284206.1:c.663-10225_663-10221del	NM_001284206.1:c.663-10224_663-10221del	NM_001284206.1:c.663-10223_663-10221del	NM_001284206.1:c.663-10222_663-10221del	NM_001284206.1:c.663-10221del	NM_001284206.1:c.663-10221dup	NM_001284206.1:c.663-10222_663-10221dup	NM_001284206.1:c.663-10223_663-10221dup	NM_001284206.1:c.663-10224_663-10221dup	NM_001284206.1:c.663-10225_663-10221dup	NM_001284206.1:c.663-10227_663-10221dup
DCAF5 transcript variant 3	NM_001284207.1:c.420-10221=	NM_001284207.1:c.420-10227_420-10221del	NM_001284207.1:c.420-10226_420-10221del	NM_001284207.1:c.420-10225_420-10221del	NM_001284207.1:c.420-10224_420-10221del	NM_001284207.1:c.420-10223_420-10221del	NM_001284207.1:c.420-10222_420-10221del	NM_001284207.1:c.420-10221del	NM_001284207.1:c.420-10221dup	NM_001284207.1:c.420-10222_420-10221dup	NM_001284207.1:c.420-10223_420-10221dup	NM_001284207.1:c.420-10224_420-10221dup	NM_001284207.1:c.420-10225_420-10221dup	NM_001284207.1:c.420-10227_420-10221dup
DCAF5 transcript variant 4	NM_001284208.2:c.666-10221=	NM_001284208.2:c.666-10227_666-10221del	NM_001284208.2:c.666-10226_666-10221del	NM_001284208.2:c.666-10225_666-10221del	NM_001284208.2:c.666-10224_666-10221del	NM_001284208.2:c.666-10223_666-10221del	NM_001284208.2:c.666-10222_666-10221del	NM_001284208.2:c.666-10221del	NM_001284208.2:c.666-10221dup	NM_001284208.2:c.666-10222_666-10221dup	NM_001284208.2:c.666-10223_666-10221dup	NM_001284208.2:c.666-10224_666-10221dup	NM_001284208.2:c.666-10225_666-10221dup	NM_001284208.2:c.666-10227_666-10221dup
DCAF5 transcript variant 1	NM_003861.2:c.666-10221=	NM_003861.2:c.666-10227_666-10221del	NM_003861.2:c.666-10226_666-10221del	NM_003861.2:c.666-10225_666-10221del	NM_003861.2:c.666-10224_666-10221del	NM_003861.2:c.666-10223_666-10221del	NM_003861.2:c.666-10222_666-10221del	NM_003861.2:c.666-10221del	NM_003861.2:c.666-10221dup	NM_003861.2:c.666-10222_666-10221dup	NM_003861.2:c.666-10223_666-10221dup	NM_003861.2:c.666-10224_666-10221dup	NM_003861.2:c.666-10225_666-10221dup	NM_003861.2:c.666-10227_666-10221dup
DCAF5 transcript variant 1	NM_003861.3:c.666-10221=	NM_003861.3:c.666-10227_666-10221del	NM_003861.3:c.666-10226_666-10221del	NM_003861.3:c.666-10225_666-10221del	NM_003861.3:c.666-10224_666-10221del	NM_003861.3:c.666-10223_666-10221del	NM_003861.3:c.666-10222_666-10221del	NM_003861.3:c.666-10221del	NM_003861.3:c.666-10221dup	NM_003861.3:c.666-10222_666-10221dup	NM_003861.3:c.666-10223_666-10221dup	NM_003861.3:c.666-10224_666-10221dup	NM_003861.3:c.666-10225_666-10221dup	NM_003861.3:c.666-10227_666-10221dup
DCAF5 transcript variant X1	XM_005268161.1:c.663-10221=	XM_005268161.1:c.663-10227_663-10221del	XM_005268161.1:c.663-10226_663-10221del	XM_005268161.1:c.663-10225_663-10221del	XM_005268161.1:c.663-10224_663-10221del	XM_005268161.1:c.663-10223_663-10221del	XM_005268161.1:c.663-10222_663-10221del	XM_005268161.1:c.663-10221del	XM_005268161.1:c.663-10221dup	XM_005268161.1:c.663-10222_663-10221dup	XM_005268161.1:c.663-10223_663-10221dup	XM_005268161.1:c.663-10224_663-10221dup	XM_005268161.1:c.663-10225_663-10221dup	XM_005268161.1:c.663-10227_663-10221dup
DCAF5 transcript variant X2	XM_005268162.1:c.420-10221=	XM_005268162.1:c.420-10227_420-10221del	XM_005268162.1:c.420-10226_420-10221del	XM_005268162.1:c.420-10225_420-10221del	XM_005268162.1:c.420-10224_420-10221del	XM_005268162.1:c.420-10223_420-10221del	XM_005268162.1:c.420-10222_420-10221del	XM_005268162.1:c.420-10221del	XM_005268162.1:c.420-10221dup	XM_005268162.1:c.420-10222_420-10221dup	XM_005268162.1:c.420-10223_420-10221dup	XM_005268162.1:c.420-10224_420-10221dup	XM_005268162.1:c.420-10225_420-10221dup	XM_005268162.1:c.420-10227_420-10221dup
DCAF5 transcript variant X4	XM_005268164.1:c.-233-10221=	XM_005268164.1:c.-233-10227_-233-10221del	XM_005268164.1:c.-233-10226_-233-10221del	XM_005268164.1:c.-233-10225_-233-10221del	XM_005268164.1:c.-233-10224_-233-10221del	XM_005268164.1:c.-233-10223_-233-10221del	XM_005268164.1:c.-233-10222_-233-10221del	XM_005268164.1:c.-233-10221del	XM_005268164.1:c.-233-10221dup	XM_005268164.1:c.-233-10222_-233-10221dup	XM_005268164.1:c.-233-10223_-233-10221dup	XM_005268164.1:c.-233-10224_-233-10221dup	XM_005268164.1:c.-233-10225_-233-10221dup	XM_005268164.1:c.-233-10227_-233-10221dup
DCAF5 transcript variant X1	XM_006720297.3:c.666-10221=	XM_006720297.3:c.666-10227_666-10221del	XM_006720297.3:c.666-10226_666-10221del	XM_006720297.3:c.666-10225_666-10221del	XM_006720297.3:c.666-10224_666-10221del	XM_006720297.3:c.666-10223_666-10221del	XM_006720297.3:c.666-10222_666-10221del	XM_006720297.3:c.666-10221del	XM_006720297.3:c.666-10221dup	XM_006720297.3:c.666-10222_666-10221dup	XM_006720297.3:c.666-10223_666-10221dup	XM_006720297.3:c.666-10224_666-10221dup	XM_006720297.3:c.666-10225_666-10221dup	XM_006720297.3:c.666-10227_666-10221dup
DCAF5 transcript variant X2	XM_006720298.3:c.663-10221=	XM_006720298.3:c.663-10227_663-10221del	XM_006720298.3:c.663-10226_663-10221del	XM_006720298.3:c.663-10225_663-10221del	XM_006720298.3:c.663-10224_663-10221del	XM_006720298.3:c.663-10223_663-10221del	XM_006720298.3:c.663-10222_663-10221del	XM_006720298.3:c.663-10221del	XM_006720298.3:c.663-10221dup	XM_006720298.3:c.663-10222_663-10221dup	XM_006720298.3:c.663-10223_663-10221dup	XM_006720298.3:c.663-10224_663-10221dup	XM_006720298.3:c.663-10225_663-10221dup	XM_006720298.3:c.663-10227_663-10221dup
DCAF5 transcript variant X3	XM_006720299.4:c.420-10221=	XM_006720299.4:c.420-10227_420-10221del	XM_006720299.4:c.420-10226_420-10221del	XM_006720299.4:c.420-10225_420-10221del	XM_006720299.4:c.420-10224_420-10221del	XM_006720299.4:c.420-10223_420-10221del	XM_006720299.4:c.420-10222_420-10221del	XM_006720299.4:c.420-10221del	XM_006720299.4:c.420-10221dup	XM_006720299.4:c.420-10222_420-10221dup	XM_006720299.4:c.420-10223_420-10221dup	XM_006720299.4:c.420-10224_420-10221dup	XM_006720299.4:c.420-10225_420-10221dup	XM_006720299.4:c.420-10227_420-10221dup
DCAF5 transcript variant X7	XM_011537278.2:c.420-10221=	XM_011537278.2:c.420-10227_420-10221del	XM_011537278.2:c.420-10226_420-10221del	XM_011537278.2:c.420-10225_420-10221del	XM_011537278.2:c.420-10224_420-10221del	XM_011537278.2:c.420-10223_420-10221del	XM_011537278.2:c.420-10222_420-10221del	XM_011537278.2:c.420-10221del	XM_011537278.2:c.420-10221dup	XM_011537278.2:c.420-10222_420-10221dup	XM_011537278.2:c.420-10223_420-10221dup	XM_011537278.2:c.420-10224_420-10221dup	XM_011537278.2:c.420-10225_420-10221dup	XM_011537278.2:c.420-10227_420-10221dup
DCAF5 transcript variant X4	XM_011537279.3:c.420-10221=	XM_011537279.3:c.420-10227_420-10221del	XM_011537279.3:c.420-10226_420-10221del	XM_011537279.3:c.420-10225_420-10221del	XM_011537279.3:c.420-10224_420-10221del	XM_011537279.3:c.420-10223_420-10221del	XM_011537279.3:c.420-10222_420-10221del	XM_011537279.3:c.420-10221del	XM_011537279.3:c.420-10221dup	XM_011537279.3:c.420-10222_420-10221dup	XM_011537279.3:c.420-10223_420-10221dup	XM_011537279.3:c.420-10224_420-10221dup	XM_011537279.3:c.420-10225_420-10221dup	XM_011537279.3:c.420-10227_420-10221dup
DCAF5 transcript variant X9	XM_011537280.4:c.15-10221=	XM_011537280.4:c.15-10227_15-10221del	XM_011537280.4:c.15-10226_15-10221del	XM_011537280.4:c.15-10225_15-10221del	XM_011537280.4:c.15-10224_15-10221del	XM_011537280.4:c.15-10223_15-10221del	XM_011537280.4:c.15-10222_15-10221del	XM_011537280.4:c.15-10221del	XM_011537280.4:c.15-10221dup	XM_011537280.4:c.15-10222_15-10221dup	XM_011537280.4:c.15-10223_15-10221dup	XM_011537280.4:c.15-10224_15-10221dup	XM_011537280.4:c.15-10225_15-10221dup	XM_011537280.4:c.15-10227_15-10221dup
DCAF5 transcript variant X5	XM_017021733.2:c.420-10221=	XM_017021733.2:c.420-10227_420-10221del	XM_017021733.2:c.420-10226_420-10221del	XM_017021733.2:c.420-10225_420-10221del	XM_017021733.2:c.420-10224_420-10221del	XM_017021733.2:c.420-10223_420-10221del	XM_017021733.2:c.420-10222_420-10221del	XM_017021733.2:c.420-10221del	XM_017021733.2:c.420-10221dup	XM_017021733.2:c.420-10222_420-10221dup	XM_017021733.2:c.420-10223_420-10221dup	XM_017021733.2:c.420-10224_420-10221dup	XM_017021733.2:c.420-10225_420-10221dup	XM_017021733.2:c.420-10227_420-10221dup
DCAF5 transcript variant X10	XM_017021737.2:c.15-10221=	XM_017021737.2:c.15-10227_15-10221del	XM_017021737.2:c.15-10226_15-10221del	XM_017021737.2:c.15-10225_15-10221del	XM_017021737.2:c.15-10224_15-10221del	XM_017021737.2:c.15-10223_15-10221del	XM_017021737.2:c.15-10222_15-10221del	XM_017021737.2:c.15-10221del	XM_017021737.2:c.15-10221dup	XM_017021737.2:c.15-10222_15-10221dup	XM_017021737.2:c.15-10223_15-10221dup	XM_017021737.2:c.15-10224_15-10221dup	XM_017021737.2:c.15-10225_15-10221dup	XM_017021737.2:c.15-10227_15-10221dup
DCAF5 transcript variant X6	XM_047431846.1:c.420-10221=	XM_047431846.1:c.420-10227_420-10221del	XM_047431846.1:c.420-10226_420-10221del	XM_047431846.1:c.420-10225_420-10221del	XM_047431846.1:c.420-10224_420-10221del	XM_047431846.1:c.420-10223_420-10221del	XM_047431846.1:c.420-10222_420-10221del	XM_047431846.1:c.420-10221del	XM_047431846.1:c.420-10221dup	XM_047431846.1:c.420-10222_420-10221dup	XM_047431846.1:c.420-10223_420-10221dup	XM_047431846.1:c.420-10224_420-10221dup	XM_047431846.1:c.420-10225_420-10221dup	XM_047431846.1:c.420-10227_420-10221dup
DCAF5 transcript variant X8	XM_047431847.1:c.420-10221=	XM_047431847.1:c.420-10227_420-10221del	XM_047431847.1:c.420-10226_420-10221del	XM_047431847.1:c.420-10225_420-10221del	XM_047431847.1:c.420-10224_420-10221del	XM_047431847.1:c.420-10223_420-10221del	XM_047431847.1:c.420-10222_420-10221del	XM_047431847.1:c.420-10221del	XM_047431847.1:c.420-10221dup	XM_047431847.1:c.420-10222_420-10221dup	XM_047431847.1:c.420-10223_420-10221dup	XM_047431847.1:c.420-10224_420-10221dup	XM_047431847.1:c.420-10225_420-10221dup	XM_047431847.1:c.420-10227_420-10221dup

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#.

40 SubSNP, 19 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294837163	May 09, 2011 (134)
2	1000GENOMES	ss1374235301	Aug 21, 2014 (142)
3	SWEGEN	ss3012398126	Nov 08, 2017 (151)
4	SWEGEN	ss3012398127	Nov 08, 2017 (151)
5	MCHAISSO	ss3064633266	Nov 08, 2017 (151)
6	EVA_DECODE	ss3696917400	Jul 13, 2019 (153)
7	EVA_DECODE	ss3696917401	Jul 13, 2019 (153)
8	EVA_DECODE	ss3696917402	Jul 13, 2019 (153)
9	EVA_DECODE	ss3696917403	Jul 13, 2019 (153)
10	PACBIO	ss3787698863	Jul 13, 2019 (153)
11	KHV_HUMAN_GENOMES	ss3817800030	Jul 13, 2019 (153)
12	EVA	ss3833980630	Apr 27, 2020 (154)
13	EVA	ss3846071031	Apr 27, 2020 (154)
14	GNOMAD	ss4280140936	Apr 26, 2021 (155)
15	GNOMAD	ss4280140937	Apr 26, 2021 (155)
16	GNOMAD	ss4280140938	Apr 26, 2021 (155)
17	GNOMAD	ss4280140939	Apr 26, 2021 (155)
18	GNOMAD	ss4280140940	Apr 26, 2021 (155)
19	GNOMAD	ss4280140942	Apr 26, 2021 (155)
20	GNOMAD	ss4280140943	Apr 26, 2021 (155)
21	GNOMAD	ss4280140944	Apr 26, 2021 (155)
22	GNOMAD	ss4280140945	Apr 26, 2021 (155)
23	GNOMAD	ss4280140946	Apr 26, 2021 (155)
24	GNOMAD	ss4280140947	Apr 26, 2021 (155)
25	GNOMAD	ss4280140948	Apr 26, 2021 (155)
26	TOMMO_GENOMICS	ss5213777818	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5213777819	Apr 26, 2021 (155)
28	TOMMO_GENOMICS	ss5213777820	Apr 26, 2021 (155)
29	1000G_HIGH_COVERAGE	ss5296646069	Oct 16, 2022 (156)
30	1000G_HIGH_COVERAGE	ss5296646070	Oct 16, 2022 (156)
31	1000G_HIGH_COVERAGE	ss5296646071	Oct 16, 2022 (156)
32	1000G_HIGH_COVERAGE	ss5296646072	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5296646073	Oct 16, 2022 (156)
34	HUGCELL_USP	ss5490647665	Oct 16, 2022 (156)
35	HUGCELL_USP	ss5490647666	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5490647667	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5490647668	Oct 16, 2022 (156)
38	HUGCELL_USP	ss5490647669	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5766738152	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5766738153	Oct 16, 2022 (156)
41	1000Genomes	NC_000014.8 - 69568825	Oct 12, 2018 (152)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 454683882 (NC_000014.9:69102107::T 36047/121928) Row 454683883 (NC_000014.9:69102107::TT 354/121932) Row 454683884 (NC_000014.9:69102107::TTT 14/121952)...	-	Apr 26, 2021 (155)
54	8.3KJPN Submission ignored due to conflicting rows: Row 71747125 (NC_000014.8:69568824:T: 325/16760) Row 71747126 (NC_000014.8:69568824::T 25/16760) Row 71747127 (NC_000014.8:69568824:TT: 2/16760)	-	Apr 26, 2021 (155)
55	8.3KJPN Submission ignored due to conflicting rows: Row 71747125 (NC_000014.8:69568824:T: 325/16760) Row 71747126 (NC_000014.8:69568824::T 25/16760) Row 71747127 (NC_000014.8:69568824:TT: 2/16760)	-	Apr 26, 2021 (155)
56	8.3KJPN Submission ignored due to conflicting rows: Row 71747125 (NC_000014.8:69568824:T: 325/16760) Row 71747126 (NC_000014.8:69568824::T 25/16760) Row 71747127 (NC_000014.8:69568824:TT: 2/16760)	-	Apr 26, 2021 (155)
57	14KJPN Submission ignored due to conflicting rows: Row 100575256 (NC_000014.9:69102107:T: 536/28258) Row 100575257 (NC_000014.9:69102107::T 48/28258)	-	Oct 16, 2022 (156)
58	14KJPN Submission ignored due to conflicting rows: Row 100575256 (NC_000014.9:69102107:T: 536/28258) Row 100575257 (NC_000014.9:69102107::T 48/28258)	-	Oct 16, 2022 (156)
59	ALFA	NC_000014.9 - 69102108	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
ss4280140948	NC_000014.9:69102107:TTTTTTT:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4280140947	NC_000014.9:69102107:TTTTTT:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4280140946	NC_000014.9:69102107:TTTTT:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4280140945	NC_000014.9:69102107:TTTT:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4280140944, ss5296646070, ss5490647669	NC_000014.9:69102107:TTT:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5213777820	NC_000014.8:69568824:TT:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4280140943, ss5296646072, ss5490647665	NC_000014.9:69102107:TT:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
64485181, ss1374235301, ss3787698863, ss5213777818	NC_000014.8:69568824:T:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3696917400, ss3817800030, ss4280140942, ss5296646071, ss5490647668, ss5766738152	NC_000014.9:69102107:T:	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss294837163	NC_000014.7:68638578::T	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3012398126, ss3833980630, ss5213777819	NC_000014.8:69568824::T	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3064633266, ss3846071031, ss4280140936, ss5296646069, ss5490647666, ss5766738153	NC_000014.9:69102107::T	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3696917401	NC_000014.9:69102108::T	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3012398127	NC_000014.8:69568824::TT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4280140937, ss5296646073, ss5490647667	NC_000014.9:69102107::TT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
5980433599	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3696917402	NC_000014.9:69102108::TT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4280140938	NC_000014.9:69102107::TTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280140939	NC_000014.9:69102107::TTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4280140940	NC_000014.9:69102107::TTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3696917403	NC_000014.9:69102108::TTTTTTT	NC_000014.9:69102107:TTTTTTTTTTTTT… NC_000014.9:69102107:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs141874345

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

rs141874345