Name: rs34406567
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.

rs34406567

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:86875703-86875725 (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)₁₂ / del(T)₁₀ / del(T)₉ / de…
del(T)₁₂ / del(T)₁₀ / del(T)₉ / 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 / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄ / dup(T)₁₅ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / dup(T)₁₉ / ins(T)₄₁ / ins(T)₄₄
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.2947 (1511/5128, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: C4orf36 : 500B Downstream 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	5128	TTTTTTTTTTTTTTTTTTTTTTT=0.5333	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.2947, TTTTTTTTTTTTTTTTTTTTTTTTT=0.1455, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0064, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0082, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0068, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0051, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.535446	0.216434	0.24812	32
European	Sub	4896	TTTTTTTTTTTTTTTTTTTTTTT=0.5123	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.3078, TTTTTTTTTTTTTTTTTTTTTTTTT=0.1522, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0067, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0086, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0071, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0053, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.50601	0.230109	0.263881	32
African	Sub	98	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	96	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	10	TTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTTTTTTTTT=0	TTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	8	TTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	80	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	34	TTTTTTTTTTTTTTTTTTTTTTT=0.85	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.12, TTTTTTTTTTTTTTTTTTTTTTTTT=0.03, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.875	0.0625	0.0625	4

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	5128	(T)₂₃=0.5333	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.2947, dupTT=0.1455, dupTTT=0.0064, dup(T)₄=0.0000, dup(T)₁₀=0.0068, dup(T)₁₁=0.0051, dup(T)₁₇=0.0082
Allele Frequency Aggregator	European	Sub	4896	(T)₂₃=0.5123	del(T)₁₂=0.0000, del(T)₁₀=0.0000, del(T)₉=0.0000, del(T)₈=0.0000, del(T)₇=0.0000, del(T)₆=0.0000, del(T)₅=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0000, dupT=0.3078, dupTT=0.1522, dupTTT=0.0067, dup(T)₄=0.0000, dup(T)₁₀=0.0071, dup(T)₁₁=0.0053, dup(T)₁₇=0.0086
Allele Frequency Aggregator	African	Sub	98	(T)₂₃=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=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)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	80	(T)₂₃=1.00	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=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)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₇=0.00
Allele Frequency Aggregator	Other	Sub	34	(T)₂₃=0.85	del(T)₁₂=0.00, del(T)₁₀=0.00, del(T)₉=0.00, del(T)₈=0.00, del(T)₇=0.00, del(T)₆=0.00, del(T)₅=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.12, dupTT=0.03, dupTTT=0.00, dup(T)₄=0.00, dup(T)₁₀=0.00, dup(T)₁₁=0.00, dup(T)₁₇=0.00
Allele Frequency Aggregator	Asian	Sub	10	(T)₂₃=1.0	del(T)₁₂=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₁₀=0.0, dup(T)₁₁=0.0, dup(T)₁₇=0.0
Allele Frequency Aggregator	Latin American 1	Sub	8	(T)₂₃=1.0	del(T)₁₂=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₁₀=0.0, dup(T)₁₁=0.0, dup(T)₁₇=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₂₃=1.0	del(T)₁₂=0.0, del(T)₁₀=0.0, del(T)₉=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₁₀=0.0, dup(T)₁₁=0.0, dup(T)₁₇=0.0

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.86875714_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875716_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875717_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875718_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875719_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875720_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875721_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875722_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875723_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875724_86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875725del
GRCh38.p14 chr 4	NC_000004.12:g.86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875724_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875723_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875722_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875720_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875719_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875718_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875717_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875716_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875715_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875714_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875713_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875712_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875711_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875710_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875709_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875708_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875707_86875725dup
GRCh38.p14 chr 4	NC_000004.12:g.86875725_86875726insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.86875725_86875726insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.87796867_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796869_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796870_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796871_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796872_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796873_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796874_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796875_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796876_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796877_87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796878del
GRCh37.p13 chr 4	NC_000004.11:g.87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796877_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796876_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796875_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796873_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796872_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796871_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796870_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796869_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796868_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796867_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796866_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796865_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796864_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796863_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796862_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796861_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796860_87796878dup
GRCh37.p13 chr 4	NC_000004.11:g.87796878_87796879insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.87796878_87796879insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: C4orf36, chromosome 4 open reading frame 36 (minus strand) : 500B Downstream Variant

Molecule type	Change	Amino acid[Codon]	SO Term
C4orf36 transcript variant 1	NM_144645.4:c.	N/A	Downstream Transcript Variant
C4orf36 transcript variant 2	NM_001369888.1:c.	N/A	N/A
C4orf36 transcript variant 3	NM_001369889.1:c.	N/A	N/A
C4orf36 transcript variant X1	XM_011531612.4:c.	N/A	N/A
C4orf36 transcript variant X3	XM_011531613.4:c.	N/A	N/A
C4orf36 transcript variant X4	XM_011531615.4:c.	N/A	N/A
C4orf36 transcript variant X2	XM_017007746.3:c.	N/A	N/A

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)₂₃=	del(T)₁₂	del(T)₁₀	del(T)₉	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	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄	dup(T)₁₅	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	dup(T)₁₉	ins(T)₄₁	ins(T)₄₄
GRCh38.p14 chr 4	NC_000004.12:g.86875703_86875725=	NC_000004.12:g.86875714_86875725del	NC_000004.12:g.86875716_86875725del	NC_000004.12:g.86875717_86875725del	NC_000004.12:g.86875718_86875725del	NC_000004.12:g.86875719_86875725del	NC_000004.12:g.86875720_86875725del	NC_000004.12:g.86875721_86875725del	NC_000004.12:g.86875722_86875725del	NC_000004.12:g.86875723_86875725del	NC_000004.12:g.86875724_86875725del	NC_000004.12:g.86875725del	NC_000004.12:g.86875725dup	NC_000004.12:g.86875724_86875725dup	NC_000004.12:g.86875723_86875725dup	NC_000004.12:g.86875722_86875725dup	NC_000004.12:g.86875720_86875725dup	NC_000004.12:g.86875719_86875725dup	NC_000004.12:g.86875718_86875725dup	NC_000004.12:g.86875717_86875725dup	NC_000004.12:g.86875716_86875725dup	NC_000004.12:g.86875715_86875725dup	NC_000004.12:g.86875714_86875725dup	NC_000004.12:g.86875713_86875725dup	NC_000004.12:g.86875712_86875725dup	NC_000004.12:g.86875711_86875725dup	NC_000004.12:g.86875710_86875725dup	NC_000004.12:g.86875709_86875725dup	NC_000004.12:g.86875708_86875725dup	NC_000004.12:g.86875707_86875725dup	NC_000004.12:g.86875725_86875726insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.86875725_86875726insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.87796856_87796878=	NC_000004.11:g.87796867_87796878del	NC_000004.11:g.87796869_87796878del	NC_000004.11:g.87796870_87796878del	NC_000004.11:g.87796871_87796878del	NC_000004.11:g.87796872_87796878del	NC_000004.11:g.87796873_87796878del	NC_000004.11:g.87796874_87796878del	NC_000004.11:g.87796875_87796878del	NC_000004.11:g.87796876_87796878del	NC_000004.11:g.87796877_87796878del	NC_000004.11:g.87796878del	NC_000004.11:g.87796878dup	NC_000004.11:g.87796877_87796878dup	NC_000004.11:g.87796876_87796878dup	NC_000004.11:g.87796875_87796878dup	NC_000004.11:g.87796873_87796878dup	NC_000004.11:g.87796872_87796878dup	NC_000004.11:g.87796871_87796878dup	NC_000004.11:g.87796870_87796878dup	NC_000004.11:g.87796869_87796878dup	NC_000004.11:g.87796868_87796878dup	NC_000004.11:g.87796867_87796878dup	NC_000004.11:g.87796866_87796878dup	NC_000004.11:g.87796865_87796878dup	NC_000004.11:g.87796864_87796878dup	NC_000004.11:g.87796863_87796878dup	NC_000004.11:g.87796862_87796878dup	NC_000004.11:g.87796861_87796878dup	NC_000004.11:g.87796860_87796878dup	NC_000004.11:g.87796878_87796879insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.87796878_87796879insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

58 SubSNP, 41 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42211083	Mar 13, 2006 (126)
2	HUMANGENOME_JCVI	ss95361527	Oct 12, 2018 (152)
3	SWEGEN	ss2995067110	Nov 08, 2017 (151)
4	SWEGEN	ss2995067111	Nov 08, 2017 (151)
5	SWEGEN	ss2995067112	Nov 08, 2017 (151)
6	SWEGEN	ss2995067113	Nov 08, 2017 (151)
7	PACBIO	ss3790228314	Jul 13, 2019 (153)
8	PACBIO	ss3790228315	Jul 13, 2019 (153)
9	PACBIO	ss3795103675	Jul 13, 2019 (153)
10	PACBIO	ss3795103676	Jul 13, 2019 (153)
11	EVA	ss3828658589	Apr 26, 2020 (154)
12	GNOMAD	ss4115185393	Apr 26, 2021 (155)
13	GNOMAD	ss4115185394	Apr 26, 2021 (155)
14	GNOMAD	ss4115185395	Apr 26, 2021 (155)
15	GNOMAD	ss4115185397	Apr 26, 2021 (155)
16	GNOMAD	ss4115185398	Apr 26, 2021 (155)
17	GNOMAD	ss4115185399	Apr 26, 2021 (155)
18	GNOMAD	ss4115185400	Apr 26, 2021 (155)
19	GNOMAD	ss4115185401	Apr 26, 2021 (155)
20	GNOMAD	ss4115185402	Apr 26, 2021 (155)
21	GNOMAD	ss4115185403	Apr 26, 2021 (155)
22	GNOMAD	ss4115185404	Apr 26, 2021 (155)
23	GNOMAD	ss4115185405	Apr 26, 2021 (155)
24	GNOMAD	ss4115185406	Apr 26, 2021 (155)
25	GNOMAD	ss4115185407	Apr 26, 2021 (155)
26	GNOMAD	ss4115185408	Apr 26, 2021 (155)
27	GNOMAD	ss4115185409	Apr 26, 2021 (155)
28	GNOMAD	ss4115185410	Apr 26, 2021 (155)
29	GNOMAD	ss4115185411	Apr 26, 2021 (155)
30	GNOMAD	ss4115185412	Apr 26, 2021 (155)
31	GNOMAD	ss4115185413	Apr 26, 2021 (155)
32	GNOMAD	ss4115185415	Apr 26, 2021 (155)
33	GNOMAD	ss4115185416	Apr 26, 2021 (155)
34	GNOMAD	ss4115185417	Apr 26, 2021 (155)
35	GNOMAD	ss4115185418	Apr 26, 2021 (155)
36	GNOMAD	ss4115185419	Apr 26, 2021 (155)
37	GNOMAD	ss4115185420	Apr 26, 2021 (155)
38	GNOMAD	ss4115185421	Apr 26, 2021 (155)
39	GNOMAD	ss4115185422	Apr 26, 2021 (155)
40	GNOMAD	ss4115185423	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5166698144	Apr 26, 2021 (155)
42	TOMMO_GENOMICS	ss5166698145	Apr 26, 2021 (155)
43	TOMMO_GENOMICS	ss5166698146	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5166698147	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5166698148	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5166698149	Apr 26, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5259982517	Oct 17, 2022 (156)
48	1000G_HIGH_COVERAGE	ss5259982518	Oct 17, 2022 (156)
49	1000G_HIGH_COVERAGE	ss5259982519	Oct 17, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5259982520	Oct 17, 2022 (156)
51	HUGCELL_USP	ss5458657635	Oct 17, 2022 (156)
52	HUGCELL_USP	ss5458657636	Oct 17, 2022 (156)
53	HUGCELL_USP	ss5458657637	Oct 17, 2022 (156)
54	TOMMO_GENOMICS	ss5701320600	Oct 17, 2022 (156)
55	TOMMO_GENOMICS	ss5701320601	Oct 17, 2022 (156)
56	TOMMO_GENOMICS	ss5701320602	Oct 17, 2022 (156)
57	TOMMO_GENOMICS	ss5701320603	Oct 17, 2022 (156)
58	TOMMO_GENOMICS	ss5701320604	Oct 17, 2022 (156)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 156260921 (NC_000004.12:86875702::T 32396/66928) Row 156260922 (NC_000004.12:86875702::TT 15623/66624) Row 156260923 (NC_000004.12:86875702::TTT 581/66656)...	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 24667451 (NC_000004.11:87796855:TTTTTT: 242/16528) Row 24667452 (NC_000004.11:87796855::T 7845/16528) Row 24667453 (NC_000004.11:87796855::TT 841/16528)...	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 24667451 (NC_000004.11:87796855:TTTTTT: 242/16528) Row 24667452 (NC_000004.11:87796855::T 7845/16528) Row 24667453 (NC_000004.11:87796855::TT 841/16528)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 24667451 (NC_000004.11:87796855:TTTTTT: 242/16528) Row 24667452 (NC_000004.11:87796855::T 7845/16528) Row 24667453 (NC_000004.11:87796855::TT 841/16528)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 24667451 (NC_000004.11:87796855:TTTTTT: 242/16528) Row 24667452 (NC_000004.11:87796855::T 7845/16528) Row 24667453 (NC_000004.11:87796855::TT 841/16528)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 24667451 (NC_000004.11:87796855:TTTTTT: 242/16528) Row 24667452 (NC_000004.11:87796855::T 7845/16528) Row 24667453 (NC_000004.11:87796855::TT 841/16528)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 24667451 (NC_000004.11:87796855:TTTTTT: 242/16528) Row 24667452 (NC_000004.11:87796855::T 7845/16528) Row 24667453 (NC_000004.11:87796855::TT 841/16528)...	-	Apr 26, 2021 (155)
94	14KJPN Submission ignored due to conflicting rows: Row 35157704 (NC_000004.12:86875702::T 14193/28196) Row 35157705 (NC_000004.12:86875702::TT 1392/28196) Row 35157706 (NC_000004.12:86875702:TTTTTT: 423/28196)...	-	Oct 17, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 35157704 (NC_000004.12:86875702::T 14193/28196) Row 35157705 (NC_000004.12:86875702::TT 1392/28196) Row 35157706 (NC_000004.12:86875702:TTTTTT: 423/28196)...	-	Oct 17, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 35157704 (NC_000004.12:86875702::T 14193/28196) Row 35157705 (NC_000004.12:86875702::TT 1392/28196) Row 35157706 (NC_000004.12:86875702:TTTTTT: 423/28196)...	-	Oct 17, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 35157704 (NC_000004.12:86875702::T 14193/28196) Row 35157705 (NC_000004.12:86875702::TT 1392/28196) Row 35157706 (NC_000004.12:86875702:TTTTTT: 423/28196)...	-	Oct 17, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 35157704 (NC_000004.12:86875702::T 14193/28196) Row 35157705 (NC_000004.12:86875702::TT 1392/28196) Row 35157706 (NC_000004.12:86875702:TTTTTT: 423/28196)...	-	Oct 17, 2022 (156)
99	ALFA	NC_000004.12 - 86875703	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
ss4115185423	NC_000004.12:86875702:TTTTTTTTTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4115185422, ss5259982519	NC_000004.12:86875702:TTTTTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4115185421	NC_000004.12:86875702:TTTTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss5166698144	NC_000004.11:87796855:TTTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4115185420, ss5259982520, ss5701320602	NC_000004.12:86875702:TTTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5166698148	NC_000004.11:87796855:TTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4115185419, ss5701320603	NC_000004.12:86875702:TTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4115185418	NC_000004.12:86875702:TTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4115185417	NC_000004.12:86875702:TTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4115185416	NC_000004.12:86875702:TT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185415, ss5458657636	NC_000004.12:86875702:T:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss2995067110, ss3790228314, ss3795103675, ss5166698145	NC_000004.11:87796855::T	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185393, ss5458657635, ss5701320600	NC_000004.12:86875702::T	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2995067111, ss3790228315, ss3795103676, ss3828658589, ss5166698146	NC_000004.11:87796855::TT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185394, ss5259982517, ss5458657637, ss5701320601	NC_000004.12:86875702::TT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss42211083	NT_016354.19:12344576::TT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss95361527	NT_016354.19:12344599::TT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5166698147	NC_000004.11:87796855::TTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185395, ss5259982518	NC_000004.12:86875702::TTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185397	NC_000004.12:86875702::TTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185398	NC_000004.12:86875702::TTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185399	NC_000004.12:86875702::TTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185400	NC_000004.12:86875702::TTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185401	NC_000004.12:86875702::TTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2995067112, ss5166698149	NC_000004.11:87796855::TTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185402, ss5701320604	NC_000004.12:86875702::TTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss2995067113	NC_000004.11:87796855::TTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185403	NC_000004.12:86875702::TTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185404	NC_000004.12:86875702::TTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185405	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185406	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185407	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185408	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185409	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
10975433510	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185410	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185411	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185412	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4115185413	NC_000004.12:86875702::TTTTTTTTTTT… NC_000004.12:86875702::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3434932427	NC_000004.12:86875702:TTTTTTTTT:	NC_000004.12:86875702:TTTTTTTTTTTT… NC_000004.12:86875702:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT

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

No publications for rs34406567

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs34406567