Name: rs34257045
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.

rs34257045

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:102515108-102515128 (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)₁₀ / del(T)₈ / del(T)₇ / del…
del(T)₁₀ / del(T)₈ / del(T)₇ / del(T)₆ / del(T)₅ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₂₁
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₀=0.0000 (0/8328, ALFA)
del(T)₈=0.0000 (0/8328, ALFA)
del(T)₅=0.0000 (0/8328, ALFA) (+ 10 more)
delTTT=0.0000 (0/8328, ALFA)
delTT=0.0000 (0/8328, ALFA)
delT=0.0000 (0/8328, ALFA)
dupT=0.0000 (0/8328, ALFA)
dupTT=0.0000 (0/8328, ALFA)
dupTTT=0.0000 (0/8328, ALFA)
dup(T)₄=0.0000 (0/8328, ALFA)
dup(T)₅=0.0000 (0/8328, ALFA)
dup(T)₆=0.0000 (0/8328, ALFA)
dup(T)₇=0.0000 (0/8328, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NFKB1 : 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	8328	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	6072	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	1202	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	46	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	1156	TTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	82	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	60	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	96	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	486	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	68	TTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	322	TTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	8328	(T)₂₁=1.0000	del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	European	Sub	6072	(T)₂₁=1.0000	del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	African	Sub	1202	(T)₂₁=1.0000	del(T)₁₀=0.0000, del(T)₈=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	486	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	322	(T)₂₁=1.000	del(T)₁₀=0.000, del(T)₈=0.000, del(T)₅=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Latin American 1	Sub	96	(T)₂₁=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Asian	Sub	82	(T)₂₁=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	68	(T)₂₁=1.00	del(T)₁₀=0.00, del(T)₈=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=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 4	NC_000004.12:g.102515119_102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515121_102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515122_102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515123_102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515124_102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515126_102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515127_102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515128del
GRCh38.p14 chr 4	NC_000004.12:g.102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515127_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515126_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515125_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515124_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515123_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515122_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515121_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515119_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515118_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515117_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515116_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515115_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515114_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515113_102515128dup
GRCh38.p14 chr 4	NC_000004.12:g.102515108_102515128dup
GRCh37.p13 chr 4	NC_000004.11:g.103436276_103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436278_103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436279_103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436280_103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436281_103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436283_103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436284_103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436285del
GRCh37.p13 chr 4	NC_000004.11:g.103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436284_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436283_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436282_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436281_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436280_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436279_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436278_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436276_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436275_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436274_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436273_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436272_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436271_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436270_103436285dup
GRCh37.p13 chr 4	NC_000004.11:g.103436265_103436285dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18791_18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18793_18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18794_18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18795_18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18796_18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18798_18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18799_18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18800del
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18799_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18798_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18797_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18796_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18795_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18794_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18793_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18791_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18790_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18789_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18788_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18787_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18786_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18785_18800dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18780_18800dup

Gene: NFKB1, nuclear factor kappa B subunit 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NFKB1 transcript variant 2	NM_001165412.2:c.-7-10393… NM_001165412.2:c.-7-10393_-7-10384del	N/A	Intron Variant
NFKB1 transcript variant 3	NM_001319226.2:c.-7-10393… NM_001319226.2:c.-7-10393_-7-10384del	N/A	Intron Variant
NFKB1 transcript variant 4	NM_001382625.1:c.-8+4170_… NM_001382625.1:c.-8+4170_-8+4179del	N/A	Intron Variant
NFKB1 transcript variant 5	NM_001382626.1:c.-8+4170_… NM_001382626.1:c.-8+4170_-8+4179del	N/A	Intron Variant
NFKB1 transcript variant 6	NM_001382627.1:c.-8+4170_… NM_001382627.1:c.-8+4170_-8+4179del	N/A	Intron Variant
NFKB1 transcript variant 7	NM_001382628.1:c.-1+13331… NM_001382628.1:c.-1+13331_-1+13340del	N/A	Intron Variant
NFKB1 transcript variant 1	NM_003998.4:c.-7-10393_-7… NM_003998.4:c.-7-10393_-7-10384del	N/A	Intron Variant
NFKB1 transcript variant X3	XM_024454069.2:c.17+4170_… XM_024454069.2:c.17+4170_17+4179del	N/A	Intron Variant
NFKB1 transcript variant X2	XM_047415742.1:c.-7-10393… XM_047415742.1:c.-7-10393_-7-10384del	N/A	Intron Variant
NFKB1 transcript variant X1	XM_024454068.1:c.	N/A	Genic Upstream Transcript Variant
NFKB1 transcript variant X4	XM_047415743.1:c.	N/A	Genic Upstream Transcript Variant
NFKB1 transcript variant X5	XM_047415744.1:c.	N/A	Genic Upstream Transcript 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)₂₁=	del(T)₁₀	del(T)₈	del(T)₇	del(T)₆	del(T)₅	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₂₁
GRCh38.p14 chr 4	NC_000004.12:g.102515108_102515128=	NC_000004.12:g.102515119_102515128del	NC_000004.12:g.102515121_102515128del	NC_000004.12:g.102515122_102515128del	NC_000004.12:g.102515123_102515128del	NC_000004.12:g.102515124_102515128del	NC_000004.12:g.102515126_102515128del	NC_000004.12:g.102515127_102515128del	NC_000004.12:g.102515128del	NC_000004.12:g.102515128dup	NC_000004.12:g.102515127_102515128dup	NC_000004.12:g.102515126_102515128dup	NC_000004.12:g.102515125_102515128dup	NC_000004.12:g.102515124_102515128dup	NC_000004.12:g.102515123_102515128dup	NC_000004.12:g.102515122_102515128dup	NC_000004.12:g.102515121_102515128dup	NC_000004.12:g.102515119_102515128dup	NC_000004.12:g.102515118_102515128dup	NC_000004.12:g.102515117_102515128dup	NC_000004.12:g.102515116_102515128dup	NC_000004.12:g.102515115_102515128dup	NC_000004.12:g.102515114_102515128dup	NC_000004.12:g.102515113_102515128dup	NC_000004.12:g.102515108_102515128dup
GRCh37.p13 chr 4	NC_000004.11:g.103436265_103436285=	NC_000004.11:g.103436276_103436285del	NC_000004.11:g.103436278_103436285del	NC_000004.11:g.103436279_103436285del	NC_000004.11:g.103436280_103436285del	NC_000004.11:g.103436281_103436285del	NC_000004.11:g.103436283_103436285del	NC_000004.11:g.103436284_103436285del	NC_000004.11:g.103436285del	NC_000004.11:g.103436285dup	NC_000004.11:g.103436284_103436285dup	NC_000004.11:g.103436283_103436285dup	NC_000004.11:g.103436282_103436285dup	NC_000004.11:g.103436281_103436285dup	NC_000004.11:g.103436280_103436285dup	NC_000004.11:g.103436279_103436285dup	NC_000004.11:g.103436278_103436285dup	NC_000004.11:g.103436276_103436285dup	NC_000004.11:g.103436275_103436285dup	NC_000004.11:g.103436274_103436285dup	NC_000004.11:g.103436273_103436285dup	NC_000004.11:g.103436272_103436285dup	NC_000004.11:g.103436271_103436285dup	NC_000004.11:g.103436270_103436285dup	NC_000004.11:g.103436265_103436285dup
NFKB1 RefSeqGene (LRG_1316)	NG_050628.1:g.18780_18800=	NG_050628.1:g.18791_18800del	NG_050628.1:g.18793_18800del	NG_050628.1:g.18794_18800del	NG_050628.1:g.18795_18800del	NG_050628.1:g.18796_18800del	NG_050628.1:g.18798_18800del	NG_050628.1:g.18799_18800del	NG_050628.1:g.18800del	NG_050628.1:g.18800dup	NG_050628.1:g.18799_18800dup	NG_050628.1:g.18798_18800dup	NG_050628.1:g.18797_18800dup	NG_050628.1:g.18796_18800dup	NG_050628.1:g.18795_18800dup	NG_050628.1:g.18794_18800dup	NG_050628.1:g.18793_18800dup	NG_050628.1:g.18791_18800dup	NG_050628.1:g.18790_18800dup	NG_050628.1:g.18789_18800dup	NG_050628.1:g.18788_18800dup	NG_050628.1:g.18787_18800dup	NG_050628.1:g.18786_18800dup	NG_050628.1:g.18785_18800dup	NG_050628.1:g.18780_18800dup
NFKB1 transcript variant 2	NM_001165412.1:c.-7-10404=	NM_001165412.1:c.-7-10393_-7-10384del	NM_001165412.1:c.-7-10391_-7-10384del	NM_001165412.1:c.-7-10390_-7-10384del	NM_001165412.1:c.-7-10389_-7-10384del	NM_001165412.1:c.-7-10388_-7-10384del	NM_001165412.1:c.-7-10386_-7-10384del	NM_001165412.1:c.-7-10385_-7-10384del	NM_001165412.1:c.-7-10384del	NM_001165412.1:c.-7-10384dup	NM_001165412.1:c.-7-10385_-7-10384dup	NM_001165412.1:c.-7-10386_-7-10384dup	NM_001165412.1:c.-7-10387_-7-10384dup	NM_001165412.1:c.-7-10388_-7-10384dup	NM_001165412.1:c.-7-10389_-7-10384dup	NM_001165412.1:c.-7-10390_-7-10384dup	NM_001165412.1:c.-7-10391_-7-10384dup	NM_001165412.1:c.-7-10393_-7-10384dup	NM_001165412.1:c.-7-10394_-7-10384dup	NM_001165412.1:c.-7-10395_-7-10384dup	NM_001165412.1:c.-7-10396_-7-10384dup	NM_001165412.1:c.-7-10397_-7-10384dup	NM_001165412.1:c.-7-10398_-7-10384dup	NM_001165412.1:c.-7-10399_-7-10384dup	NM_001165412.1:c.-7-10404_-7-10384dup
NFKB1 transcript variant 2	NM_001165412.2:c.-7-10404=	NM_001165412.2:c.-7-10393_-7-10384del	NM_001165412.2:c.-7-10391_-7-10384del	NM_001165412.2:c.-7-10390_-7-10384del	NM_001165412.2:c.-7-10389_-7-10384del	NM_001165412.2:c.-7-10388_-7-10384del	NM_001165412.2:c.-7-10386_-7-10384del	NM_001165412.2:c.-7-10385_-7-10384del	NM_001165412.2:c.-7-10384del	NM_001165412.2:c.-7-10384dup	NM_001165412.2:c.-7-10385_-7-10384dup	NM_001165412.2:c.-7-10386_-7-10384dup	NM_001165412.2:c.-7-10387_-7-10384dup	NM_001165412.2:c.-7-10388_-7-10384dup	NM_001165412.2:c.-7-10389_-7-10384dup	NM_001165412.2:c.-7-10390_-7-10384dup	NM_001165412.2:c.-7-10391_-7-10384dup	NM_001165412.2:c.-7-10393_-7-10384dup	NM_001165412.2:c.-7-10394_-7-10384dup	NM_001165412.2:c.-7-10395_-7-10384dup	NM_001165412.2:c.-7-10396_-7-10384dup	NM_001165412.2:c.-7-10397_-7-10384dup	NM_001165412.2:c.-7-10398_-7-10384dup	NM_001165412.2:c.-7-10399_-7-10384dup	NM_001165412.2:c.-7-10404_-7-10384dup
NFKB1 transcript variant 3	NM_001319226.2:c.-7-10404=	NM_001319226.2:c.-7-10393_-7-10384del	NM_001319226.2:c.-7-10391_-7-10384del	NM_001319226.2:c.-7-10390_-7-10384del	NM_001319226.2:c.-7-10389_-7-10384del	NM_001319226.2:c.-7-10388_-7-10384del	NM_001319226.2:c.-7-10386_-7-10384del	NM_001319226.2:c.-7-10385_-7-10384del	NM_001319226.2:c.-7-10384del	NM_001319226.2:c.-7-10384dup	NM_001319226.2:c.-7-10385_-7-10384dup	NM_001319226.2:c.-7-10386_-7-10384dup	NM_001319226.2:c.-7-10387_-7-10384dup	NM_001319226.2:c.-7-10388_-7-10384dup	NM_001319226.2:c.-7-10389_-7-10384dup	NM_001319226.2:c.-7-10390_-7-10384dup	NM_001319226.2:c.-7-10391_-7-10384dup	NM_001319226.2:c.-7-10393_-7-10384dup	NM_001319226.2:c.-7-10394_-7-10384dup	NM_001319226.2:c.-7-10395_-7-10384dup	NM_001319226.2:c.-7-10396_-7-10384dup	NM_001319226.2:c.-7-10397_-7-10384dup	NM_001319226.2:c.-7-10398_-7-10384dup	NM_001319226.2:c.-7-10399_-7-10384dup	NM_001319226.2:c.-7-10404_-7-10384dup
NFKB1 transcript variant 4	NM_001382625.1:c.-8+4159=	NM_001382625.1:c.-8+4170_-8+4179del	NM_001382625.1:c.-8+4172_-8+4179del	NM_001382625.1:c.-8+4173_-8+4179del	NM_001382625.1:c.-8+4174_-8+4179del	NM_001382625.1:c.-8+4175_-8+4179del	NM_001382625.1:c.-8+4177_-8+4179del	NM_001382625.1:c.-8+4178_-8+4179del	NM_001382625.1:c.-8+4179del	NM_001382625.1:c.-8+4179dup	NM_001382625.1:c.-8+4178_-8+4179dup	NM_001382625.1:c.-8+4177_-8+4179dup	NM_001382625.1:c.-8+4176_-8+4179dup	NM_001382625.1:c.-8+4175_-8+4179dup	NM_001382625.1:c.-8+4174_-8+4179dup	NM_001382625.1:c.-8+4173_-8+4179dup	NM_001382625.1:c.-8+4172_-8+4179dup	NM_001382625.1:c.-8+4170_-8+4179dup	NM_001382625.1:c.-8+4169_-8+4179dup	NM_001382625.1:c.-8+4168_-8+4179dup	NM_001382625.1:c.-8+4167_-8+4179dup	NM_001382625.1:c.-8+4166_-8+4179dup	NM_001382625.1:c.-8+4165_-8+4179dup	NM_001382625.1:c.-8+4164_-8+4179dup	NM_001382625.1:c.-8+4159_-8+4179dup
NFKB1 transcript variant 5	NM_001382626.1:c.-8+4159=	NM_001382626.1:c.-8+4170_-8+4179del	NM_001382626.1:c.-8+4172_-8+4179del	NM_001382626.1:c.-8+4173_-8+4179del	NM_001382626.1:c.-8+4174_-8+4179del	NM_001382626.1:c.-8+4175_-8+4179del	NM_001382626.1:c.-8+4177_-8+4179del	NM_001382626.1:c.-8+4178_-8+4179del	NM_001382626.1:c.-8+4179del	NM_001382626.1:c.-8+4179dup	NM_001382626.1:c.-8+4178_-8+4179dup	NM_001382626.1:c.-8+4177_-8+4179dup	NM_001382626.1:c.-8+4176_-8+4179dup	NM_001382626.1:c.-8+4175_-8+4179dup	NM_001382626.1:c.-8+4174_-8+4179dup	NM_001382626.1:c.-8+4173_-8+4179dup	NM_001382626.1:c.-8+4172_-8+4179dup	NM_001382626.1:c.-8+4170_-8+4179dup	NM_001382626.1:c.-8+4169_-8+4179dup	NM_001382626.1:c.-8+4168_-8+4179dup	NM_001382626.1:c.-8+4167_-8+4179dup	NM_001382626.1:c.-8+4166_-8+4179dup	NM_001382626.1:c.-8+4165_-8+4179dup	NM_001382626.1:c.-8+4164_-8+4179dup	NM_001382626.1:c.-8+4159_-8+4179dup
NFKB1 transcript variant 6	NM_001382627.1:c.-8+4159=	NM_001382627.1:c.-8+4170_-8+4179del	NM_001382627.1:c.-8+4172_-8+4179del	NM_001382627.1:c.-8+4173_-8+4179del	NM_001382627.1:c.-8+4174_-8+4179del	NM_001382627.1:c.-8+4175_-8+4179del	NM_001382627.1:c.-8+4177_-8+4179del	NM_001382627.1:c.-8+4178_-8+4179del	NM_001382627.1:c.-8+4179del	NM_001382627.1:c.-8+4179dup	NM_001382627.1:c.-8+4178_-8+4179dup	NM_001382627.1:c.-8+4177_-8+4179dup	NM_001382627.1:c.-8+4176_-8+4179dup	NM_001382627.1:c.-8+4175_-8+4179dup	NM_001382627.1:c.-8+4174_-8+4179dup	NM_001382627.1:c.-8+4173_-8+4179dup	NM_001382627.1:c.-8+4172_-8+4179dup	NM_001382627.1:c.-8+4170_-8+4179dup	NM_001382627.1:c.-8+4169_-8+4179dup	NM_001382627.1:c.-8+4168_-8+4179dup	NM_001382627.1:c.-8+4167_-8+4179dup	NM_001382627.1:c.-8+4166_-8+4179dup	NM_001382627.1:c.-8+4165_-8+4179dup	NM_001382627.1:c.-8+4164_-8+4179dup	NM_001382627.1:c.-8+4159_-8+4179dup
NFKB1 transcript variant 7	NM_001382628.1:c.-1+13320=	NM_001382628.1:c.-1+13331_-1+13340del	NM_001382628.1:c.-1+13333_-1+13340del	NM_001382628.1:c.-1+13334_-1+13340del	NM_001382628.1:c.-1+13335_-1+13340del	NM_001382628.1:c.-1+13336_-1+13340del	NM_001382628.1:c.-1+13338_-1+13340del	NM_001382628.1:c.-1+13339_-1+13340del	NM_001382628.1:c.-1+13340del	NM_001382628.1:c.-1+13340dup	NM_001382628.1:c.-1+13339_-1+13340dup	NM_001382628.1:c.-1+13338_-1+13340dup	NM_001382628.1:c.-1+13337_-1+13340dup	NM_001382628.1:c.-1+13336_-1+13340dup	NM_001382628.1:c.-1+13335_-1+13340dup	NM_001382628.1:c.-1+13334_-1+13340dup	NM_001382628.1:c.-1+13333_-1+13340dup	NM_001382628.1:c.-1+13331_-1+13340dup	NM_001382628.1:c.-1+13330_-1+13340dup	NM_001382628.1:c.-1+13329_-1+13340dup	NM_001382628.1:c.-1+13328_-1+13340dup	NM_001382628.1:c.-1+13327_-1+13340dup	NM_001382628.1:c.-1+13326_-1+13340dup	NM_001382628.1:c.-1+13325_-1+13340dup	NM_001382628.1:c.-1+13320_-1+13340dup
NFKB1 transcript variant 1	NM_003998.3:c.-7-10404=	NM_003998.3:c.-7-10393_-7-10384del	NM_003998.3:c.-7-10391_-7-10384del	NM_003998.3:c.-7-10390_-7-10384del	NM_003998.3:c.-7-10389_-7-10384del	NM_003998.3:c.-7-10388_-7-10384del	NM_003998.3:c.-7-10386_-7-10384del	NM_003998.3:c.-7-10385_-7-10384del	NM_003998.3:c.-7-10384del	NM_003998.3:c.-7-10384dup	NM_003998.3:c.-7-10385_-7-10384dup	NM_003998.3:c.-7-10386_-7-10384dup	NM_003998.3:c.-7-10387_-7-10384dup	NM_003998.3:c.-7-10388_-7-10384dup	NM_003998.3:c.-7-10389_-7-10384dup	NM_003998.3:c.-7-10390_-7-10384dup	NM_003998.3:c.-7-10391_-7-10384dup	NM_003998.3:c.-7-10393_-7-10384dup	NM_003998.3:c.-7-10394_-7-10384dup	NM_003998.3:c.-7-10395_-7-10384dup	NM_003998.3:c.-7-10396_-7-10384dup	NM_003998.3:c.-7-10397_-7-10384dup	NM_003998.3:c.-7-10398_-7-10384dup	NM_003998.3:c.-7-10399_-7-10384dup	NM_003998.3:c.-7-10404_-7-10384dup
NFKB1 transcript variant 1	NM_003998.4:c.-7-10404=	NM_003998.4:c.-7-10393_-7-10384del	NM_003998.4:c.-7-10391_-7-10384del	NM_003998.4:c.-7-10390_-7-10384del	NM_003998.4:c.-7-10389_-7-10384del	NM_003998.4:c.-7-10388_-7-10384del	NM_003998.4:c.-7-10386_-7-10384del	NM_003998.4:c.-7-10385_-7-10384del	NM_003998.4:c.-7-10384del	NM_003998.4:c.-7-10384dup	NM_003998.4:c.-7-10385_-7-10384dup	NM_003998.4:c.-7-10386_-7-10384dup	NM_003998.4:c.-7-10387_-7-10384dup	NM_003998.4:c.-7-10388_-7-10384dup	NM_003998.4:c.-7-10389_-7-10384dup	NM_003998.4:c.-7-10390_-7-10384dup	NM_003998.4:c.-7-10391_-7-10384dup	NM_003998.4:c.-7-10393_-7-10384dup	NM_003998.4:c.-7-10394_-7-10384dup	NM_003998.4:c.-7-10395_-7-10384dup	NM_003998.4:c.-7-10396_-7-10384dup	NM_003998.4:c.-7-10397_-7-10384dup	NM_003998.4:c.-7-10398_-7-10384dup	NM_003998.4:c.-7-10399_-7-10384dup	NM_003998.4:c.-7-10404_-7-10384dup
NFKB1 transcript variant X1	XM_005263029.1:c.17+4159=	XM_005263029.1:c.17+4170_17+4179del	XM_005263029.1:c.17+4172_17+4179del	XM_005263029.1:c.17+4173_17+4179del	XM_005263029.1:c.17+4174_17+4179del	XM_005263029.1:c.17+4175_17+4179del	XM_005263029.1:c.17+4177_17+4179del	XM_005263029.1:c.17+4178_17+4179del	XM_005263029.1:c.17+4179del	XM_005263029.1:c.17+4179dup	XM_005263029.1:c.17+4178_17+4179dup	XM_005263029.1:c.17+4177_17+4179dup	XM_005263029.1:c.17+4176_17+4179dup	XM_005263029.1:c.17+4175_17+4179dup	XM_005263029.1:c.17+4174_17+4179dup	XM_005263029.1:c.17+4173_17+4179dup	XM_005263029.1:c.17+4172_17+4179dup	XM_005263029.1:c.17+4170_17+4179dup	XM_005263029.1:c.17+4169_17+4179dup	XM_005263029.1:c.17+4168_17+4179dup	XM_005263029.1:c.17+4167_17+4179dup	XM_005263029.1:c.17+4166_17+4179dup	XM_005263029.1:c.17+4165_17+4179dup	XM_005263029.1:c.17+4164_17+4179dup	XM_005263029.1:c.17+4159_17+4179dup
NFKB1 transcript variant X3	XM_024454069.2:c.17+4159=	XM_024454069.2:c.17+4170_17+4179del	XM_024454069.2:c.17+4172_17+4179del	XM_024454069.2:c.17+4173_17+4179del	XM_024454069.2:c.17+4174_17+4179del	XM_024454069.2:c.17+4175_17+4179del	XM_024454069.2:c.17+4177_17+4179del	XM_024454069.2:c.17+4178_17+4179del	XM_024454069.2:c.17+4179del	XM_024454069.2:c.17+4179dup	XM_024454069.2:c.17+4178_17+4179dup	XM_024454069.2:c.17+4177_17+4179dup	XM_024454069.2:c.17+4176_17+4179dup	XM_024454069.2:c.17+4175_17+4179dup	XM_024454069.2:c.17+4174_17+4179dup	XM_024454069.2:c.17+4173_17+4179dup	XM_024454069.2:c.17+4172_17+4179dup	XM_024454069.2:c.17+4170_17+4179dup	XM_024454069.2:c.17+4169_17+4179dup	XM_024454069.2:c.17+4168_17+4179dup	XM_024454069.2:c.17+4167_17+4179dup	XM_024454069.2:c.17+4166_17+4179dup	XM_024454069.2:c.17+4165_17+4179dup	XM_024454069.2:c.17+4164_17+4179dup	XM_024454069.2:c.17+4159_17+4179dup
NFKB1 transcript variant X2	XM_047415742.1:c.-7-10404=	XM_047415742.1:c.-7-10393_-7-10384del	XM_047415742.1:c.-7-10391_-7-10384del	XM_047415742.1:c.-7-10390_-7-10384del	XM_047415742.1:c.-7-10389_-7-10384del	XM_047415742.1:c.-7-10388_-7-10384del	XM_047415742.1:c.-7-10386_-7-10384del	XM_047415742.1:c.-7-10385_-7-10384del	XM_047415742.1:c.-7-10384del	XM_047415742.1:c.-7-10384dup	XM_047415742.1:c.-7-10385_-7-10384dup	XM_047415742.1:c.-7-10386_-7-10384dup	XM_047415742.1:c.-7-10387_-7-10384dup	XM_047415742.1:c.-7-10388_-7-10384dup	XM_047415742.1:c.-7-10389_-7-10384dup	XM_047415742.1:c.-7-10390_-7-10384dup	XM_047415742.1:c.-7-10391_-7-10384dup	XM_047415742.1:c.-7-10393_-7-10384dup	XM_047415742.1:c.-7-10394_-7-10384dup	XM_047415742.1:c.-7-10395_-7-10384dup	XM_047415742.1:c.-7-10396_-7-10384dup	XM_047415742.1:c.-7-10397_-7-10384dup	XM_047415742.1:c.-7-10398_-7-10384dup	XM_047415742.1:c.-7-10399_-7-10384dup	XM_047415742.1:c.-7-10404_-7-10384dup

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#.

41 SubSNP, 32 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42260595	Mar 13, 2006 (126)
2	HGSV	ss80239209	Oct 12, 2018 (152)
3	HUMANGENOME_JCVI	ss95364259	Dec 05, 2013 (138)
4	DDI	ss1536420887	Apr 01, 2015 (144)
5	URBANLAB	ss3647807702	Oct 12, 2018 (152)
6	EVA_DECODE	ss3712701098	Jul 13, 2019 (153)
7	EVA_DECODE	ss3712701100	Jul 13, 2019 (153)
8	EVA_DECODE	ss3712701101	Jul 13, 2019 (153)
9	EVA_DECODE	ss3712701102	Jul 13, 2019 (153)
10	EVA_DECODE	ss3712701103	Jul 13, 2019 (153)
11	GNOMAD	ss4117120389	Apr 26, 2021 (155)
12	GNOMAD	ss4117120391	Apr 26, 2021 (155)
13	GNOMAD	ss4117120396	Apr 26, 2021 (155)
14	GNOMAD	ss4117120397	Apr 26, 2021 (155)
15	GNOMAD	ss4117120398	Apr 26, 2021 (155)
16	GNOMAD	ss4117120400	Apr 26, 2021 (155)
17	GNOMAD	ss4117120401	Apr 26, 2021 (155)
18	GNOMAD	ss4117120402	Apr 26, 2021 (155)
19	GNOMAD	ss4117120403	Apr 26, 2021 (155)
20	GNOMAD	ss4117120404	Apr 26, 2021 (155)
21	GNOMAD	ss4117120405	Apr 26, 2021 (155)
22	GNOMAD	ss4117120406	Apr 26, 2021 (155)
23	GNOMAD	ss4117120407	Apr 26, 2021 (155)
24	GNOMAD	ss4117120408	Apr 26, 2021 (155)
25	GNOMAD	ss4117120409	Apr 26, 2021 (155)
26	GNOMAD	ss4117120410	Apr 26, 2021 (155)
27	GNOMAD	ss4117120411	Apr 26, 2021 (155)
28	GNOMAD	ss4117120412	Apr 26, 2021 (155)
29	GNOMAD	ss4117120413	Apr 26, 2021 (155)
30	GNOMAD	ss4117120414	Apr 26, 2021 (155)
31	GNOMAD	ss4117120415	Apr 26, 2021 (155)
32	GNOMAD	ss4117120416	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5167173369	Apr 26, 2021 (155)
34	TOMMO_GENOMICS	ss5167173370	Apr 26, 2021 (155)
35	TOMMO_GENOMICS	ss5167173371	Apr 26, 2021 (155)
36	TOMMO_GENOMICS	ss5167173372	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5167173373	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5701931380	Oct 17, 2022 (156)
39	TOMMO_GENOMICS	ss5701931381	Oct 17, 2022 (156)
40	TOMMO_GENOMICS	ss5701931383	Oct 17, 2022 (156)
41	TOMMO_GENOMICS	ss5701931384	Oct 17, 2022 (156)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 159481699 (NC_000004.12:102515107::T 1063/87864) Row 159481701 (NC_000004.12:102515107::TT 575/87860) Row 159481706 (NC_000004.12:102515107::TTT 1679/87800)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 25142676 (NC_000004.11:103436264::TTTTTT 36/14354) Row 25142677 (NC_000004.11:103436264::TTT 126/14354) Row 25142678 (NC_000004.11:103436264:T: 1390/14354)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 25142676 (NC_000004.11:103436264::TTTTTT 36/14354) Row 25142677 (NC_000004.11:103436264::TTT 126/14354) Row 25142678 (NC_000004.11:103436264:T: 1390/14354)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 25142676 (NC_000004.11:103436264::TTTTTT 36/14354) Row 25142677 (NC_000004.11:103436264::TTT 126/14354) Row 25142678 (NC_000004.11:103436264:T: 1390/14354)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 25142676 (NC_000004.11:103436264::TTTTTT 36/14354) Row 25142677 (NC_000004.11:103436264::TTT 126/14354) Row 25142678 (NC_000004.11:103436264:T: 1390/14354)...	-	Apr 26, 2021 (155)
68	8.3KJPN Submission ignored due to conflicting rows: Row 25142676 (NC_000004.11:103436264::TTTTTT 36/14354) Row 25142677 (NC_000004.11:103436264::TTT 126/14354) Row 25142678 (NC_000004.11:103436264:T: 1390/14354)...	-	Apr 26, 2021 (155)
69	14KJPN Submission ignored due to conflicting rows: Row 35768484 (NC_000004.12:102515107:T: 2740/24222) Row 35768485 (NC_000004.12:102515107::TTT 220/24222) Row 35768487 (NC_000004.12:102515107::TTTTTT 80/24222)...	-	Oct 17, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 35768484 (NC_000004.12:102515107:T: 2740/24222) Row 35768485 (NC_000004.12:102515107::TTT 220/24222) Row 35768487 (NC_000004.12:102515107::TTTTTT 80/24222)...	-	Oct 17, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 35768484 (NC_000004.12:102515107:T: 2740/24222) Row 35768485 (NC_000004.12:102515107::TTT 220/24222) Row 35768487 (NC_000004.12:102515107::TTTTTT 80/24222)...	-	Oct 17, 2022 (156)
72	14KJPN Submission ignored due to conflicting rows: Row 35768484 (NC_000004.12:102515107:T: 2740/24222) Row 35768485 (NC_000004.12:102515107::TTT 220/24222) Row 35768487 (NC_000004.12:102515107::TTTTTT 80/24222)...	-	Oct 17, 2022 (156)
73	ALFA	NC_000004.12 - 102515108	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Associated ID	History Updated (Build)
rs70937552	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4117120416	NC_000004.12:102515107:TTTTTTTTTT:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4117120415	NC_000004.12:102515107:TTTTTTTT:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5167173373	NC_000004.11:103436264:TTTTTTT:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss3712701098	NC_000004.12:102515107:TTTTTT:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4117120414	NC_000004.12:102515107:TTTTT:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4117120413	NC_000004.12:102515107:TTT:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4117120412	NC_000004.12:102515107:TT:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss5167173371	NC_000004.11:103436264:T:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3647807702, ss4117120411, ss5701931380	NC_000004.12:102515107:T:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss42260595	NT_016354.19:27983985:T:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss95364259	NT_016354.19:27984005:T:	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss5167173372	NC_000004.11:103436264::T	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120389, ss5701931384	NC_000004.12:102515107::T	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3712701100	NC_000004.12:102515113::T	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1536420887	NC_000004.11:103436264::TT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120391	NC_000004.12:102515107::TT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss80239209	NT_016354.19:27984006::TT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5167173370	NC_000004.11:103436264::TTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120396, ss5701931381	NC_000004.12:102515107::TTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3712701101	NC_000004.12:102515113::TTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120397	NC_000004.12:102515107::TTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120398	NC_000004.12:102515107::TTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3712701102	NC_000004.12:102515113::TTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5167173369	NC_000004.11:103436264::TTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120400, ss5701931383	NC_000004.12:102515107::TTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3712701103	NC_000004.12:102515113::TTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120401	NC_000004.12:102515107::TTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7457856363	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120402	NC_000004.12:102515107::TTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120403	NC_000004.12:102515107::TTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120404	NC_000004.12:102515107::TTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120405	NC_000004.12:102515107::TTTTTTTTTT… NC_000004.12:102515107::TTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120406	NC_000004.12:102515107::TTTTTTTTTT… NC_000004.12:102515107::TTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120407	NC_000004.12:102515107::TTTTTTTTTT… NC_000004.12:102515107::TTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120408	NC_000004.12:102515107::TTTTTTTTTT… NC_000004.12:102515107::TTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120409	NC_000004.12:102515107::TTTTTTTTTT… NC_000004.12:102515107::TTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4117120410	NC_000004.12:102515107::TTTTTTTTTT… NC_000004.12:102515107::TTTTTTTTTTTTTTTTTTTTT	NC_000004.12:102515107:TTTTTTTTTTT… NC_000004.12:102515107:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs34257045

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

rs34257045