Name: rs11415941
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.

rs11415941

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr6:151321904-151321928 (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)₁₄ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₄ / del(T)₁₂ / del(T)₁₁ / 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)₅ / 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)₁₇ / ins(T)₃₃
Variation Type: Indel Insertion and Deletion
Frequency: dupTT=0.01012 (119/11760, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: AKAP12 : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

ALFA Allele Frequency
The ALFA project provide aggregate allele frequency from dbGaP. More information is available on the project page including descriptions, data access, and terms of use.

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	Alt HMOZ	HTRZ	HWEP
Total	Global	11760	TTTTTTTTTTTTTTTTTTTTTTTTT=0.97296	TTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00493, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00918, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.01012, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00230, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00051, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	0.982121	0.002454	0.015425	32
European	Sub	9900	TTTTTTTTTTTTTTTTTTTTTTTTT=0.9680	TTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0059, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0109, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0119, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0027, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0006, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.978848	0.002932	0.01822	32
African	Sub	976	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	44	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	932	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	58	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	44	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	14	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	96	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	410	TTTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	56	TTTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	264	TTTTTTTTTTTTTTTTTTTTTTTTT=0.996	TTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.004, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	0.992424	0.0	0.007576	0

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	11760	(T)₂₅=0.97296	del(T)₁₄=0.00000, del(T)₁₂=0.00000, del(T)₁₁=0.00000, del(T)₁₀=0.00000, del(T)₉=0.00000, del(T)₈=0.00000, del(T)₇=0.00000, del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00493, dupT=0.00918, dupTT=0.01012, dupTTT=0.00230, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00051
Allele Frequency Aggregator	European	Sub	9900	(T)₂₅=0.9680	del(T)₁₄=0.0000, del(T)₁₂=0.0000, del(T)₁₁=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, del(T)₄=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0059, dupT=0.0109, dupTT=0.0119, dupTTT=0.0027, dup(T)₄=0.0000, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0006
Allele Frequency Aggregator	African	Sub	976	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, 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 2	Sub	410	(T)₂₅=1.000	del(T)₁₄=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, 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	264	(T)₂₅=0.996	del(T)₁₄=0.000, del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=0.000, del(T)₉=0.000, del(T)₈=0.000, del(T)₇=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.004, 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)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=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, del(T)₄=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	58	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=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, del(T)₄=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	56	(T)₂₅=1.00	del(T)₁₄=0.00, del(T)₁₂=0.00, del(T)₁₁=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, del(T)₄=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 6	NC_000006.12:g.151321915_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321917_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321918_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321919_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321920_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321921_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321922_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321923_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321924_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321925_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321926_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321927_151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321928del
GRCh38.p14 chr 6	NC_000006.12:g.151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321927_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321926_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321925_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321924_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321923_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321922_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321921_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321920_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321919_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321918_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321917_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321916_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321915_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321912_151321928dup
GRCh38.p14 chr 6	NC_000006.12:g.151321928_151321929insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.151643050_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643052_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643053_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643054_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643055_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643056_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643057_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643058_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643059_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643060_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643061_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643062_151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643063del
GRCh37.p13 chr 6	NC_000006.11:g.151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643062_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643061_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643060_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643059_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643058_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643057_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643056_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643055_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643054_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643053_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643052_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643051_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643050_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643047_151643063dup
GRCh37.p13 chr 6	NC_000006.11:g.151643063_151643064insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
AKAP12 RefSeqGene	NG_029875.1:g.86917_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86919_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86920_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86921_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86922_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86923_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86924_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86925_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86926_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86927_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86928_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86929_86930del
AKAP12 RefSeqGene	NG_029875.1:g.86930del
AKAP12 RefSeqGene	NG_029875.1:g.86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86929_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86928_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86927_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86926_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86925_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86924_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86923_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86922_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86921_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86920_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86919_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86918_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86917_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86914_86930dup
AKAP12 RefSeqGene	NG_029875.1:g.86930_86931insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Gene: AKAP12, A-kinase anchoring protein 12 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
AKAP12 transcript variant 1	NM_005100.4:c.319+16012_3… NM_005100.4:c.319+16012_319+16025del	N/A	Intron Variant
AKAP12 transcript variant 3	NM_001370346.1:c.	N/A	Genic Upstream Transcript Variant
AKAP12 transcript variant 2	NM_144497.2:c.	N/A	Genic Upstream Transcript Variant
AKAP12 transcript variant X1	XM_017011517.3:c.319+1601… XM_017011517.3:c.319+16012_319+16025del	N/A	Intron Variant
AKAP12 transcript variant X2	XM_047419579.1: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)₂₅=	del(T)₁₄	del(T)₁₂	del(T)₁₁	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)₅	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)₁₇	ins(T)₃₃
GRCh38.p14 chr 6	NC_000006.12:g.151321904_151321928=	NC_000006.12:g.151321915_151321928del	NC_000006.12:g.151321917_151321928del	NC_000006.12:g.151321918_151321928del	NC_000006.12:g.151321919_151321928del	NC_000006.12:g.151321920_151321928del	NC_000006.12:g.151321921_151321928del	NC_000006.12:g.151321922_151321928del	NC_000006.12:g.151321923_151321928del	NC_000006.12:g.151321924_151321928del	NC_000006.12:g.151321925_151321928del	NC_000006.12:g.151321926_151321928del	NC_000006.12:g.151321927_151321928del	NC_000006.12:g.151321928del	NC_000006.12:g.151321928dup	NC_000006.12:g.151321927_151321928dup	NC_000006.12:g.151321926_151321928dup	NC_000006.12:g.151321925_151321928dup	NC_000006.12:g.151321924_151321928dup	NC_000006.12:g.151321923_151321928dup	NC_000006.12:g.151321922_151321928dup	NC_000006.12:g.151321921_151321928dup	NC_000006.12:g.151321920_151321928dup	NC_000006.12:g.151321919_151321928dup	NC_000006.12:g.151321918_151321928dup	NC_000006.12:g.151321917_151321928dup	NC_000006.12:g.151321916_151321928dup	NC_000006.12:g.151321915_151321928dup	NC_000006.12:g.151321912_151321928dup	NC_000006.12:g.151321928_151321929insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 6	NC_000006.11:g.151643039_151643063=	NC_000006.11:g.151643050_151643063del	NC_000006.11:g.151643052_151643063del	NC_000006.11:g.151643053_151643063del	NC_000006.11:g.151643054_151643063del	NC_000006.11:g.151643055_151643063del	NC_000006.11:g.151643056_151643063del	NC_000006.11:g.151643057_151643063del	NC_000006.11:g.151643058_151643063del	NC_000006.11:g.151643059_151643063del	NC_000006.11:g.151643060_151643063del	NC_000006.11:g.151643061_151643063del	NC_000006.11:g.151643062_151643063del	NC_000006.11:g.151643063del	NC_000006.11:g.151643063dup	NC_000006.11:g.151643062_151643063dup	NC_000006.11:g.151643061_151643063dup	NC_000006.11:g.151643060_151643063dup	NC_000006.11:g.151643059_151643063dup	NC_000006.11:g.151643058_151643063dup	NC_000006.11:g.151643057_151643063dup	NC_000006.11:g.151643056_151643063dup	NC_000006.11:g.151643055_151643063dup	NC_000006.11:g.151643054_151643063dup	NC_000006.11:g.151643053_151643063dup	NC_000006.11:g.151643052_151643063dup	NC_000006.11:g.151643051_151643063dup	NC_000006.11:g.151643050_151643063dup	NC_000006.11:g.151643047_151643063dup	NC_000006.11:g.151643063_151643064insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
AKAP12 RefSeqGene	NG_029875.1:g.86906_86930=	NG_029875.1:g.86917_86930del	NG_029875.1:g.86919_86930del	NG_029875.1:g.86920_86930del	NG_029875.1:g.86921_86930del	NG_029875.1:g.86922_86930del	NG_029875.1:g.86923_86930del	NG_029875.1:g.86924_86930del	NG_029875.1:g.86925_86930del	NG_029875.1:g.86926_86930del	NG_029875.1:g.86927_86930del	NG_029875.1:g.86928_86930del	NG_029875.1:g.86929_86930del	NG_029875.1:g.86930del	NG_029875.1:g.86930dup	NG_029875.1:g.86929_86930dup	NG_029875.1:g.86928_86930dup	NG_029875.1:g.86927_86930dup	NG_029875.1:g.86926_86930dup	NG_029875.1:g.86925_86930dup	NG_029875.1:g.86924_86930dup	NG_029875.1:g.86923_86930dup	NG_029875.1:g.86922_86930dup	NG_029875.1:g.86921_86930dup	NG_029875.1:g.86920_86930dup	NG_029875.1:g.86919_86930dup	NG_029875.1:g.86918_86930dup	NG_029875.1:g.86917_86930dup	NG_029875.1:g.86914_86930dup	NG_029875.1:g.86930_86931insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
AKAP12 transcript variant 1	NM_005100.3:c.319+16001=	NM_005100.3:c.319+16012_319+16025del	NM_005100.3:c.319+16014_319+16025del	NM_005100.3:c.319+16015_319+16025del	NM_005100.3:c.319+16016_319+16025del	NM_005100.3:c.319+16017_319+16025del	NM_005100.3:c.319+16018_319+16025del	NM_005100.3:c.319+16019_319+16025del	NM_005100.3:c.319+16020_319+16025del	NM_005100.3:c.319+16021_319+16025del	NM_005100.3:c.319+16022_319+16025del	NM_005100.3:c.319+16023_319+16025del	NM_005100.3:c.319+16024_319+16025del	NM_005100.3:c.319+16025del	NM_005100.3:c.319+16025dup	NM_005100.3:c.319+16024_319+16025dup	NM_005100.3:c.319+16023_319+16025dup	NM_005100.3:c.319+16022_319+16025dup	NM_005100.3:c.319+16021_319+16025dup	NM_005100.3:c.319+16020_319+16025dup	NM_005100.3:c.319+16019_319+16025dup	NM_005100.3:c.319+16018_319+16025dup	NM_005100.3:c.319+16017_319+16025dup	NM_005100.3:c.319+16016_319+16025dup	NM_005100.3:c.319+16015_319+16025dup	NM_005100.3:c.319+16014_319+16025dup	NM_005100.3:c.319+16013_319+16025dup	NM_005100.3:c.319+16012_319+16025dup	NM_005100.3:c.319+16009_319+16025dup	NM_005100.3:c.319+16025_319+16026insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
AKAP12 transcript variant 1	NM_005100.4:c.319+16001=	NM_005100.4:c.319+16012_319+16025del	NM_005100.4:c.319+16014_319+16025del	NM_005100.4:c.319+16015_319+16025del	NM_005100.4:c.319+16016_319+16025del	NM_005100.4:c.319+16017_319+16025del	NM_005100.4:c.319+16018_319+16025del	NM_005100.4:c.319+16019_319+16025del	NM_005100.4:c.319+16020_319+16025del	NM_005100.4:c.319+16021_319+16025del	NM_005100.4:c.319+16022_319+16025del	NM_005100.4:c.319+16023_319+16025del	NM_005100.4:c.319+16024_319+16025del	NM_005100.4:c.319+16025del	NM_005100.4:c.319+16025dup	NM_005100.4:c.319+16024_319+16025dup	NM_005100.4:c.319+16023_319+16025dup	NM_005100.4:c.319+16022_319+16025dup	NM_005100.4:c.319+16021_319+16025dup	NM_005100.4:c.319+16020_319+16025dup	NM_005100.4:c.319+16019_319+16025dup	NM_005100.4:c.319+16018_319+16025dup	NM_005100.4:c.319+16017_319+16025dup	NM_005100.4:c.319+16016_319+16025dup	NM_005100.4:c.319+16015_319+16025dup	NM_005100.4:c.319+16014_319+16025dup	NM_005100.4:c.319+16013_319+16025dup	NM_005100.4:c.319+16012_319+16025dup	NM_005100.4:c.319+16009_319+16025dup	NM_005100.4:c.319+16025_319+16026insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
AKAP12 transcript variant X1	XM_005267233.1:c.319+16001=	XM_005267233.1:c.319+16012_319+16025del	XM_005267233.1:c.319+16014_319+16025del	XM_005267233.1:c.319+16015_319+16025del	XM_005267233.1:c.319+16016_319+16025del	XM_005267233.1:c.319+16017_319+16025del	XM_005267233.1:c.319+16018_319+16025del	XM_005267233.1:c.319+16019_319+16025del	XM_005267233.1:c.319+16020_319+16025del	XM_005267233.1:c.319+16021_319+16025del	XM_005267233.1:c.319+16022_319+16025del	XM_005267233.1:c.319+16023_319+16025del	XM_005267233.1:c.319+16024_319+16025del	XM_005267233.1:c.319+16025del	XM_005267233.1:c.319+16025dup	XM_005267233.1:c.319+16024_319+16025dup	XM_005267233.1:c.319+16023_319+16025dup	XM_005267233.1:c.319+16022_319+16025dup	XM_005267233.1:c.319+16021_319+16025dup	XM_005267233.1:c.319+16020_319+16025dup	XM_005267233.1:c.319+16019_319+16025dup	XM_005267233.1:c.319+16018_319+16025dup	XM_005267233.1:c.319+16017_319+16025dup	XM_005267233.1:c.319+16016_319+16025dup	XM_005267233.1:c.319+16015_319+16025dup	XM_005267233.1:c.319+16014_319+16025dup	XM_005267233.1:c.319+16013_319+16025dup	XM_005267233.1:c.319+16012_319+16025dup	XM_005267233.1:c.319+16009_319+16025dup	XM_005267233.1:c.319+16025_319+16026insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
AKAP12 transcript variant X2	XM_005267234.1:c.-2136-1821=	XM_005267234.1:c.-2136-1810_-2136-1797del	XM_005267234.1:c.-2136-1808_-2136-1797del	XM_005267234.1:c.-2136-1807_-2136-1797del	XM_005267234.1:c.-2136-1806_-2136-1797del	XM_005267234.1:c.-2136-1805_-2136-1797del	XM_005267234.1:c.-2136-1804_-2136-1797del	XM_005267234.1:c.-2136-1803_-2136-1797del	XM_005267234.1:c.-2136-1802_-2136-1797del	XM_005267234.1:c.-2136-1801_-2136-1797del	XM_005267234.1:c.-2136-1800_-2136-1797del	XM_005267234.1:c.-2136-1799_-2136-1797del	XM_005267234.1:c.-2136-1798_-2136-1797del	XM_005267234.1:c.-2136-1797del	XM_005267234.1:c.-2136-1797dup	XM_005267234.1:c.-2136-1798_-2136-1797dup	XM_005267234.1:c.-2136-1799_-2136-1797dup	XM_005267234.1:c.-2136-1800_-2136-1797dup	XM_005267234.1:c.-2136-1801_-2136-1797dup	XM_005267234.1:c.-2136-1802_-2136-1797dup	XM_005267234.1:c.-2136-1803_-2136-1797dup	XM_005267234.1:c.-2136-1804_-2136-1797dup	XM_005267234.1:c.-2136-1805_-2136-1797dup	XM_005267234.1:c.-2136-1806_-2136-1797dup	XM_005267234.1:c.-2136-1807_-2136-1797dup	XM_005267234.1:c.-2136-1808_-2136-1797dup	XM_005267234.1:c.-2136-1809_-2136-1797dup	XM_005267234.1:c.-2136-1810_-2136-1797dup	XM_005267234.1:c.-2136-1813_-2136-1797dup	XM_005267234.1:c.-2136-1797_-2136-1796insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
AKAP12 transcript variant X1	XM_017011517.3:c.319+16001=	XM_017011517.3:c.319+16012_319+16025del	XM_017011517.3:c.319+16014_319+16025del	XM_017011517.3:c.319+16015_319+16025del	XM_017011517.3:c.319+16016_319+16025del	XM_017011517.3:c.319+16017_319+16025del	XM_017011517.3:c.319+16018_319+16025del	XM_017011517.3:c.319+16019_319+16025del	XM_017011517.3:c.319+16020_319+16025del	XM_017011517.3:c.319+16021_319+16025del	XM_017011517.3:c.319+16022_319+16025del	XM_017011517.3:c.319+16023_319+16025del	XM_017011517.3:c.319+16024_319+16025del	XM_017011517.3:c.319+16025del	XM_017011517.3:c.319+16025dup	XM_017011517.3:c.319+16024_319+16025dup	XM_017011517.3:c.319+16023_319+16025dup	XM_017011517.3:c.319+16022_319+16025dup	XM_017011517.3:c.319+16021_319+16025dup	XM_017011517.3:c.319+16020_319+16025dup	XM_017011517.3:c.319+16019_319+16025dup	XM_017011517.3:c.319+16018_319+16025dup	XM_017011517.3:c.319+16017_319+16025dup	XM_017011517.3:c.319+16016_319+16025dup	XM_017011517.3:c.319+16015_319+16025dup	XM_017011517.3:c.319+16014_319+16025dup	XM_017011517.3:c.319+16013_319+16025dup	XM_017011517.3:c.319+16012_319+16025dup	XM_017011517.3:c.319+16009_319+16025dup	XM_017011517.3:c.319+16025_319+16026insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

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#.

51 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss42881360	Mar 13, 2006 (137)
2	SWEGEN	ss3000190139	Nov 08, 2017 (151)
3	EVA_DECODE	ss3718575775	Jul 13, 2019 (153)
4	EVA_DECODE	ss3718575776	Jul 13, 2019 (153)
5	EVA_DECODE	ss3718575777	Jul 13, 2019 (153)
6	EVA_DECODE	ss3718575778	Jul 13, 2019 (153)
7	EVA_DECODE	ss3718575779	Jul 13, 2019 (153)
8	EVA_DECODE	ss3718575780	Jul 13, 2019 (153)
9	GNOMAD	ss4154060905	Apr 26, 2021 (155)
10	GNOMAD	ss4154060906	Apr 26, 2021 (155)
11	GNOMAD	ss4154060916	Apr 26, 2021 (155)
12	GNOMAD	ss4154060917	Apr 26, 2021 (155)
13	GNOMAD	ss4154060918	Apr 26, 2021 (155)
14	GNOMAD	ss4154060919	Apr 26, 2021 (155)
15	GNOMAD	ss4154060920	Apr 26, 2021 (155)
16	GNOMAD	ss4154060921	Apr 26, 2021 (155)
17	GNOMAD	ss4154060922	Apr 26, 2021 (155)
18	GNOMAD	ss4154060923	Apr 26, 2021 (155)
19	GNOMAD	ss4154060924	Apr 26, 2021 (155)
20	GNOMAD	ss4154060925	Apr 26, 2021 (155)
21	GNOMAD	ss4154060926	Apr 26, 2021 (155)
22	GNOMAD	ss4154060927	Apr 26, 2021 (155)
23	GNOMAD	ss4154060928	Apr 26, 2021 (155)
24	GNOMAD	ss4154060929	Apr 26, 2021 (155)
25	GNOMAD	ss4154060931	Apr 26, 2021 (155)
26	GNOMAD	ss4154060932	Apr 26, 2021 (155)
27	GNOMAD	ss4154060933	Apr 26, 2021 (155)
28	GNOMAD	ss4154060934	Apr 26, 2021 (155)
29	GNOMAD	ss4154060935	Apr 26, 2021 (155)
30	GNOMAD	ss4154060936	Apr 26, 2021 (155)
31	GNOMAD	ss4154060937	Apr 26, 2021 (155)
32	GNOMAD	ss4154060938	Apr 26, 2021 (155)
33	GNOMAD	ss4154060939	Apr 26, 2021 (155)
34	GNOMAD	ss4154060940	Apr 26, 2021 (155)
35	TOPMED	ss4727115720	Apr 26, 2021 (155)
36	TOPMED	ss4727115721	Apr 26, 2021 (155)
37	TOMMO_GENOMICS	ss5180608800	Apr 26, 2021 (155)
38	TOMMO_GENOMICS	ss5180608801	Apr 26, 2021 (155)
39	TOMMO_GENOMICS	ss5180608802	Apr 26, 2021 (155)
40	TOMMO_GENOMICS	ss5180608803	Apr 26, 2021 (155)
41	TOMMO_GENOMICS	ss5180608804	Apr 26, 2021 (155)
42	HUGCELL_USP	ss5468280466	Oct 13, 2022 (156)
43	HUGCELL_USP	ss5468280467	Oct 13, 2022 (156)
44	HUGCELL_USP	ss5468280468	Oct 13, 2022 (156)
45	HUGCELL_USP	ss5468280469	Oct 13, 2022 (156)
46	HUGCELL_USP	ss5468280470	Oct 13, 2022 (156)
47	TOMMO_GENOMICS	ss5719684668	Oct 13, 2022 (156)
48	TOMMO_GENOMICS	ss5719684669	Oct 13, 2022 (156)
49	TOMMO_GENOMICS	ss5719684670	Oct 13, 2022 (156)
50	TOMMO_GENOMICS	ss5719684672	Oct 13, 2022 (156)
51	TOMMO_GENOMICS	ss5719684673	Oct 13, 2022 (156)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 245533488 (NC_000006.12:151321903::T 6366/62228) Row 245533489 (NC_000006.12:151321903::TT 5360/61982) Row 245533499 (NC_000006.12:151321903::TTT 2261/62108)...	-	Apr 26, 2021 (155)
78	8.3KJPN Submission ignored due to conflicting rows: Row 38578107 (NC_000006.11:151643038::T 973/16584) Row 38578108 (NC_000006.11:151643038:T: 923/16584) Row 38578109 (NC_000006.11:151643038::TT 235/16584)...	-	Apr 26, 2021 (155)
79	8.3KJPN Submission ignored due to conflicting rows: Row 38578107 (NC_000006.11:151643038::T 973/16584) Row 38578108 (NC_000006.11:151643038:T: 923/16584) Row 38578109 (NC_000006.11:151643038::TT 235/16584)...	-	Apr 26, 2021 (155)
80	8.3KJPN Submission ignored due to conflicting rows: Row 38578107 (NC_000006.11:151643038::T 973/16584) Row 38578108 (NC_000006.11:151643038:T: 923/16584) Row 38578109 (NC_000006.11:151643038::TT 235/16584)...	-	Apr 26, 2021 (155)
81	8.3KJPN Submission ignored due to conflicting rows: Row 38578107 (NC_000006.11:151643038::T 973/16584) Row 38578108 (NC_000006.11:151643038:T: 923/16584) Row 38578109 (NC_000006.11:151643038::TT 235/16584)...	-	Apr 26, 2021 (155)
82	8.3KJPN Submission ignored due to conflicting rows: Row 38578107 (NC_000006.11:151643038::T 973/16584) Row 38578108 (NC_000006.11:151643038:T: 923/16584) Row 38578109 (NC_000006.11:151643038::TT 235/16584)...	-	Apr 26, 2021 (155)
83	14KJPN Submission ignored due to conflicting rows: Row 53521772 (NC_000006.12:151321903::TT 355/26986) Row 53521773 (NC_000006.12:151321903::T 1512/26986) Row 53521774 (NC_000006.12:151321903:T: 1737/26986)...	-	Oct 13, 2022 (156)
84	14KJPN Submission ignored due to conflicting rows: Row 53521772 (NC_000006.12:151321903::TT 355/26986) Row 53521773 (NC_000006.12:151321903::T 1512/26986) Row 53521774 (NC_000006.12:151321903:T: 1737/26986)...	-	Oct 13, 2022 (156)
85	14KJPN Submission ignored due to conflicting rows: Row 53521772 (NC_000006.12:151321903::TT 355/26986) Row 53521773 (NC_000006.12:151321903::T 1512/26986) Row 53521774 (NC_000006.12:151321903:T: 1737/26986)...	-	Oct 13, 2022 (156)
86	14KJPN Submission ignored due to conflicting rows: Row 53521772 (NC_000006.12:151321903::TT 355/26986) Row 53521773 (NC_000006.12:151321903::T 1512/26986) Row 53521774 (NC_000006.12:151321903:T: 1737/26986)...	-	Oct 13, 2022 (156)
87	14KJPN Submission ignored due to conflicting rows: Row 53521772 (NC_000006.12:151321903::TT 355/26986) Row 53521773 (NC_000006.12:151321903::T 1512/26986) Row 53521774 (NC_000006.12:151321903:T: 1737/26986)...	-	Oct 13, 2022 (156)
88	TopMed Submission ignored due to conflicting rows: Row 564493278 (NC_000006.12:151321903:TTTTTTTTTTTT: 15/264690) Row 564493279 (NC_000006.12:151321903:TTTTTTTTTTTTTT: 2/264690)	-	Apr 26, 2021 (155)
89	TopMed Submission ignored due to conflicting rows: Row 564493278 (NC_000006.12:151321903:TTTTTTTTTTTT: 15/264690) Row 564493279 (NC_000006.12:151321903:TTTTTTTTTTTTTT: 2/264690)	-	Apr 26, 2021 (155)
90	ALFA	NC_000006.12 - 151321904	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)
rs34488454	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss5180608804	NC_000006.11:151643038:TTTTTTTTTTT… NC_000006.11:151643038:TTTTTTTTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4727115721, ss5719684673	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4154060940, ss4727115720	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss5180608803	NC_000006.11:151643038:TTTTTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4154060939, ss5719684672	NC_000006.12:151321903:TTTTTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4154060938	NC_000006.12:151321903:TTTTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4154060937	NC_000006.12:151321903:TTTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4154060936	NC_000006.12:151321903:TTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3000190139	NC_000006.11:151643038:TTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4154060935	NC_000006.12:151321903:TTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4154060934	NC_000006.12:151321903:TTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3718575775, ss4154060933	NC_000006.12:151321903:TTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060932, ss5468280470	NC_000006.12:151321903:TT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3718575776	NC_000006.12:151321904:TT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5180608801	NC_000006.11:151643038:T:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060931, ss5468280468, ss5719684670	NC_000006.12:151321903:T:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3718575777	NC_000006.12:151321905:T:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5180608800	NC_000006.11:151643038::T	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060905, ss5468280466, ss5719684669	NC_000006.12:151321903::T	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3718575778	NC_000006.12:151321906::T	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss42881360	NT_025741.15:55812520::T	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5180608802	NC_000006.11:151643038::TT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060906, ss5468280469, ss5719684668	NC_000006.12:151321903::TT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3718575779	NC_000006.12:151321906::TT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060916, ss5468280467	NC_000006.12:151321903::TTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3718575780	NC_000006.12:151321906::TTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060917	NC_000006.12:151321903::TTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060918	NC_000006.12:151321903::TTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060919	NC_000006.12:151321903::TTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060920	NC_000006.12:151321903::TTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4463992910	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060921	NC_000006.12:151321903::TTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060922	NC_000006.12:151321903::TTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060923	NC_000006.12:151321903::TTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060924	NC_000006.12:151321903::TTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060925	NC_000006.12:151321903::TTTTTTTTTT… NC_000006.12:151321903::TTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060926	NC_000006.12:151321903::TTTTTTTTTT… NC_000006.12:151321903::TTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060927	NC_000006.12:151321903::TTTTTTTTTT… NC_000006.12:151321903::TTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060928	NC_000006.12:151321903::TTTTTTTTTT… NC_000006.12:151321903::TTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4154060929	NC_000006.12:151321903::TTTTTTTTTT… NC_000006.12:151321903::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3515859497	NC_000006.12:151321903:TTTTTTTT:	NC_000006.12:151321903:TTTTTTTTTTT… NC_000006.12:151321903:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT

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

No publications for rs11415941

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

rs11415941