Name: rs71386075
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.

rs71386075

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr16:85099798-85099821 (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)₁₅ / del(T)₁₂ / del(T)₁₁ / d…
del(T)₁₅ / 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)₁₅ / dup(T)₁₇ / dup(T)₁₈ / dup(T)₁₉
Variation Type: Indel Insertion and Deletion
Frequency: delT=0.1746 (1060/6070, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CIBAR2 : 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	6070	TTTTTTTTTTTTTTTTTTTTTTTT=0.7783	TTTTTTTTT=0.0000, TTTTTTTTTTTT=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=0.0031, TTTTTTTTTTTTTTTTTTTTTT=0.0420, TTTTTTTTTTTTTTTTTTTTTTT=0.1746, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0008, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.738833	0.088256	0.172911	32
European	Sub	5822	TTTTTTTTTTTTTTTTTTTTTTTT=0.7695	TTTTTTTTT=0.0000, TTTTTTTTTTTT=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=0.0033, TTTTTTTTTTTTTTTTTTTTTT=0.0436, TTTTTTTTTTTTTTTTTTTTTTT=0.1816, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0009, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0012, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.727478	0.092348	0.180173	32
African	Sub	106	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	104	TTTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	24	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	22	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	2	TTTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	12	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	24	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	66	TTTTTTTTTTTTTTTTTTTTTTTT=0.94	TTTTTTTTT=0.00, TTTTTTTTTTTT=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=0.02, TTTTTTTTTTTTTTTTTTTTTTT=0.05, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.9375	0.0	0.0625	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	6070	(T)₂₄=0.7783	del(T)₁₅=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=0.0031, delTT=0.0420, delT=0.1746, dupT=0.0000, dupTT=0.0000, dup(T)₁₇=0.0012, dup(T)₁₉=0.0008
Allele Frequency Aggregator	European	Sub	5822	(T)₂₄=0.7695	del(T)₁₅=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=0.0033, delTT=0.0436, delT=0.1816, dupT=0.0000, dupTT=0.0000, dup(T)₁₇=0.0012, dup(T)₁₉=0.0009
Allele Frequency Aggregator	African	Sub	106	(T)₂₄=1.000	del(T)₁₅=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, dup(T)₁₇=0.000, dup(T)₁₉=0.000
Allele Frequency Aggregator	Other	Sub	66	(T)₂₄=0.94	del(T)₁₅=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=0.02, delT=0.05, dupT=0.00, dupTT=0.00, dup(T)₁₇=0.00, dup(T)₁₉=0.00
Allele Frequency Aggregator	Latin American 2	Sub	24	(T)₂₄=1.00	del(T)₁₅=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, dup(T)₁₇=0.00, dup(T)₁₉=0.00
Allele Frequency Aggregator	Asian	Sub	24	(T)₂₄=1.00	del(T)₁₅=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, dup(T)₁₇=0.00, dup(T)₁₉=0.00
Allele Frequency Aggregator	South Asian	Sub	16	(T)₂₄=1.00	del(T)₁₅=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, dup(T)₁₇=0.00, dup(T)₁₉=0.00
Allele Frequency Aggregator	Latin American 1	Sub	12	(T)₂₄=1.00	del(T)₁₅=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, dup(T)₁₇=0.00, dup(T)₁₉=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 16	NC_000016.10:g.85099807_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099810_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099811_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099812_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099813_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099814_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099815_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099816_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099817_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099818_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099819_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099820_85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099821del
GRCh38.p14 chr 16	NC_000016.10:g.85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099820_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099819_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099818_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099817_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099816_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099815_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099814_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099813_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099812_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099807_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099805_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099804_85099821dup
GRCh38.p14 chr 16	NC_000016.10:g.85099803_85099821dup
GRCh37.p13 chr 16	NC_000016.9:g.85133413_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133416_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133417_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133418_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133419_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133420_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133421_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133422_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133423_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133424_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133425_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133426_85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133427del
GRCh37.p13 chr 16	NC_000016.9:g.85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133426_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133425_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133424_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133423_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133422_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133421_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133420_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133419_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133418_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133413_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133411_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133410_85133427dup
GRCh37.p13 chr 16	NC_000016.9:g.85133409_85133427dup

Gene: CIBAR2, CBY1 interacting BAR domain containing 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CIBAR2 transcript variant 2	NM_001366920.1:c.753+327_… NM_001366920.1:c.753+327_753+341del	N/A	Intron Variant
CIBAR2 transcript variant 1	NM_198491.3:c.753+327_753… NM_198491.3:c.753+327_753+341del	N/A	Intron Variant
CIBAR2 transcript variant X1	XM_011523063.2:c.753+327_… XM_011523063.2:c.753+327_753+341del	N/A	Intron Variant
CIBAR2 transcript variant X2	XM_017023198.2:c.753+327_… XM_017023198.2:c.753+327_753+341del	N/A	Intron Variant

Clinical Significance tab shows a list of clinical significance entries from ClinVar associated with the variation, per allele. Click on the RCV accession (i.e. RCV000001615.2) or Allele ID (i.e. 12274) to access full ClinVar report.

Not Reported in ClinVar

Aliases tab displays HGVS names representing the variant placements and allele changes on genomic, transcript and protein sequences, per allele. HGVS name is an expression for reporting sequence accession and version, sequence type, position, and allele change. The column "Note" can have two values: "diff" means that there is a difference between the reference allele (variation interval) at the placement reported in HGVS name and the reference alleles reported in other HGVS names, and "rev" means that the sequence of this variation interval at the placement reported in HGVS name is in reverse orientation to the sequence(s) of this variation in other HGVS names not labeled as "rev".

Placement	(T)₂₄=	del(T)₁₅	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)₁₅	dup(T)₁₇	dup(T)₁₈	dup(T)₁₉
GRCh38.p14 chr 16	NC_000016.10:g.85099798_85099821=	NC_000016.10:g.85099807_85099821del	NC_000016.10:g.85099810_85099821del	NC_000016.10:g.85099811_85099821del	NC_000016.10:g.85099812_85099821del	NC_000016.10:g.85099813_85099821del	NC_000016.10:g.85099814_85099821del	NC_000016.10:g.85099815_85099821del	NC_000016.10:g.85099816_85099821del	NC_000016.10:g.85099817_85099821del	NC_000016.10:g.85099818_85099821del	NC_000016.10:g.85099819_85099821del	NC_000016.10:g.85099820_85099821del	NC_000016.10:g.85099821del	NC_000016.10:g.85099821dup	NC_000016.10:g.85099820_85099821dup	NC_000016.10:g.85099819_85099821dup	NC_000016.10:g.85099818_85099821dup	NC_000016.10:g.85099817_85099821dup	NC_000016.10:g.85099816_85099821dup	NC_000016.10:g.85099815_85099821dup	NC_000016.10:g.85099814_85099821dup	NC_000016.10:g.85099813_85099821dup	NC_000016.10:g.85099812_85099821dup	NC_000016.10:g.85099807_85099821dup	NC_000016.10:g.85099805_85099821dup	NC_000016.10:g.85099804_85099821dup	NC_000016.10:g.85099803_85099821dup
GRCh37.p13 chr 16	NC_000016.9:g.85133404_85133427=	NC_000016.9:g.85133413_85133427del	NC_000016.9:g.85133416_85133427del	NC_000016.9:g.85133417_85133427del	NC_000016.9:g.85133418_85133427del	NC_000016.9:g.85133419_85133427del	NC_000016.9:g.85133420_85133427del	NC_000016.9:g.85133421_85133427del	NC_000016.9:g.85133422_85133427del	NC_000016.9:g.85133423_85133427del	NC_000016.9:g.85133424_85133427del	NC_000016.9:g.85133425_85133427del	NC_000016.9:g.85133426_85133427del	NC_000016.9:g.85133427del	NC_000016.9:g.85133427dup	NC_000016.9:g.85133426_85133427dup	NC_000016.9:g.85133425_85133427dup	NC_000016.9:g.85133424_85133427dup	NC_000016.9:g.85133423_85133427dup	NC_000016.9:g.85133422_85133427dup	NC_000016.9:g.85133421_85133427dup	NC_000016.9:g.85133420_85133427dup	NC_000016.9:g.85133419_85133427dup	NC_000016.9:g.85133418_85133427dup	NC_000016.9:g.85133413_85133427dup	NC_000016.9:g.85133411_85133427dup	NC_000016.9:g.85133410_85133427dup	NC_000016.9:g.85133409_85133427dup
CIBAR2 transcript variant 2	NM_001366920.1:c.753+341=	NM_001366920.1:c.753+327_753+341del	NM_001366920.1:c.753+330_753+341del	NM_001366920.1:c.753+331_753+341del	NM_001366920.1:c.753+332_753+341del	NM_001366920.1:c.753+333_753+341del	NM_001366920.1:c.753+334_753+341del	NM_001366920.1:c.753+335_753+341del	NM_001366920.1:c.753+336_753+341del	NM_001366920.1:c.753+337_753+341del	NM_001366920.1:c.753+338_753+341del	NM_001366920.1:c.753+339_753+341del	NM_001366920.1:c.753+340_753+341del	NM_001366920.1:c.753+341del	NM_001366920.1:c.753+341dup	NM_001366920.1:c.753+340_753+341dup	NM_001366920.1:c.753+339_753+341dup	NM_001366920.1:c.753+338_753+341dup	NM_001366920.1:c.753+337_753+341dup	NM_001366920.1:c.753+336_753+341dup	NM_001366920.1:c.753+335_753+341dup	NM_001366920.1:c.753+334_753+341dup	NM_001366920.1:c.753+333_753+341dup	NM_001366920.1:c.753+332_753+341dup	NM_001366920.1:c.753+327_753+341dup	NM_001366920.1:c.753+325_753+341dup	NM_001366920.1:c.753+324_753+341dup	NM_001366920.1:c.753+323_753+341dup
FAM92B transcript	NM_198491.1:c.753+341=	NM_198491.1:c.753+327_753+341del	NM_198491.1:c.753+330_753+341del	NM_198491.1:c.753+331_753+341del	NM_198491.1:c.753+332_753+341del	NM_198491.1:c.753+333_753+341del	NM_198491.1:c.753+334_753+341del	NM_198491.1:c.753+335_753+341del	NM_198491.1:c.753+336_753+341del	NM_198491.1:c.753+337_753+341del	NM_198491.1:c.753+338_753+341del	NM_198491.1:c.753+339_753+341del	NM_198491.1:c.753+340_753+341del	NM_198491.1:c.753+341del	NM_198491.1:c.753+341dup	NM_198491.1:c.753+340_753+341dup	NM_198491.1:c.753+339_753+341dup	NM_198491.1:c.753+338_753+341dup	NM_198491.1:c.753+337_753+341dup	NM_198491.1:c.753+336_753+341dup	NM_198491.1:c.753+335_753+341dup	NM_198491.1:c.753+334_753+341dup	NM_198491.1:c.753+333_753+341dup	NM_198491.1:c.753+332_753+341dup	NM_198491.1:c.753+327_753+341dup	NM_198491.1:c.753+325_753+341dup	NM_198491.1:c.753+324_753+341dup	NM_198491.1:c.753+323_753+341dup
CIBAR2 transcript variant 1	NM_198491.3:c.753+341=	NM_198491.3:c.753+327_753+341del	NM_198491.3:c.753+330_753+341del	NM_198491.3:c.753+331_753+341del	NM_198491.3:c.753+332_753+341del	NM_198491.3:c.753+333_753+341del	NM_198491.3:c.753+334_753+341del	NM_198491.3:c.753+335_753+341del	NM_198491.3:c.753+336_753+341del	NM_198491.3:c.753+337_753+341del	NM_198491.3:c.753+338_753+341del	NM_198491.3:c.753+339_753+341del	NM_198491.3:c.753+340_753+341del	NM_198491.3:c.753+341del	NM_198491.3:c.753+341dup	NM_198491.3:c.753+340_753+341dup	NM_198491.3:c.753+339_753+341dup	NM_198491.3:c.753+338_753+341dup	NM_198491.3:c.753+337_753+341dup	NM_198491.3:c.753+336_753+341dup	NM_198491.3:c.753+335_753+341dup	NM_198491.3:c.753+334_753+341dup	NM_198491.3:c.753+333_753+341dup	NM_198491.3:c.753+332_753+341dup	NM_198491.3:c.753+327_753+341dup	NM_198491.3:c.753+325_753+341dup	NM_198491.3:c.753+324_753+341dup	NM_198491.3:c.753+323_753+341dup
FAM92B transcript variant X2	XM_005255931.1:c.753+341=	XM_005255931.1:c.753+327_753+341del	XM_005255931.1:c.753+330_753+341del	XM_005255931.1:c.753+331_753+341del	XM_005255931.1:c.753+332_753+341del	XM_005255931.1:c.753+333_753+341del	XM_005255931.1:c.753+334_753+341del	XM_005255931.1:c.753+335_753+341del	XM_005255931.1:c.753+336_753+341del	XM_005255931.1:c.753+337_753+341del	XM_005255931.1:c.753+338_753+341del	XM_005255931.1:c.753+339_753+341del	XM_005255931.1:c.753+340_753+341del	XM_005255931.1:c.753+341del	XM_005255931.1:c.753+341dup	XM_005255931.1:c.753+340_753+341dup	XM_005255931.1:c.753+339_753+341dup	XM_005255931.1:c.753+338_753+341dup	XM_005255931.1:c.753+337_753+341dup	XM_005255931.1:c.753+336_753+341dup	XM_005255931.1:c.753+335_753+341dup	XM_005255931.1:c.753+334_753+341dup	XM_005255931.1:c.753+333_753+341dup	XM_005255931.1:c.753+332_753+341dup	XM_005255931.1:c.753+327_753+341dup	XM_005255931.1:c.753+325_753+341dup	XM_005255931.1:c.753+324_753+341dup	XM_005255931.1:c.753+323_753+341dup
CIBAR2 transcript variant X1	XM_011523063.2:c.753+341=	XM_011523063.2:c.753+327_753+341del	XM_011523063.2:c.753+330_753+341del	XM_011523063.2:c.753+331_753+341del	XM_011523063.2:c.753+332_753+341del	XM_011523063.2:c.753+333_753+341del	XM_011523063.2:c.753+334_753+341del	XM_011523063.2:c.753+335_753+341del	XM_011523063.2:c.753+336_753+341del	XM_011523063.2:c.753+337_753+341del	XM_011523063.2:c.753+338_753+341del	XM_011523063.2:c.753+339_753+341del	XM_011523063.2:c.753+340_753+341del	XM_011523063.2:c.753+341del	XM_011523063.2:c.753+341dup	XM_011523063.2:c.753+340_753+341dup	XM_011523063.2:c.753+339_753+341dup	XM_011523063.2:c.753+338_753+341dup	XM_011523063.2:c.753+337_753+341dup	XM_011523063.2:c.753+336_753+341dup	XM_011523063.2:c.753+335_753+341dup	XM_011523063.2:c.753+334_753+341dup	XM_011523063.2:c.753+333_753+341dup	XM_011523063.2:c.753+332_753+341dup	XM_011523063.2:c.753+327_753+341dup	XM_011523063.2:c.753+325_753+341dup	XM_011523063.2:c.753+324_753+341dup	XM_011523063.2:c.753+323_753+341dup
CIBAR2 transcript variant X2	XM_017023198.2:c.753+341=	XM_017023198.2:c.753+327_753+341del	XM_017023198.2:c.753+330_753+341del	XM_017023198.2:c.753+331_753+341del	XM_017023198.2:c.753+332_753+341del	XM_017023198.2:c.753+333_753+341del	XM_017023198.2:c.753+334_753+341del	XM_017023198.2:c.753+335_753+341del	XM_017023198.2:c.753+336_753+341del	XM_017023198.2:c.753+337_753+341del	XM_017023198.2:c.753+338_753+341del	XM_017023198.2:c.753+339_753+341del	XM_017023198.2:c.753+340_753+341del	XM_017023198.2:c.753+341del	XM_017023198.2:c.753+341dup	XM_017023198.2:c.753+340_753+341dup	XM_017023198.2:c.753+339_753+341dup	XM_017023198.2:c.753+338_753+341dup	XM_017023198.2:c.753+337_753+341dup	XM_017023198.2:c.753+336_753+341dup	XM_017023198.2:c.753+335_753+341dup	XM_017023198.2:c.753+334_753+341dup	XM_017023198.2:c.753+333_753+341dup	XM_017023198.2:c.753+332_753+341dup	XM_017023198.2:c.753+327_753+341dup	XM_017023198.2:c.753+325_753+341dup	XM_017023198.2:c.753+324_753+341dup	XM_017023198.2:c.753+323_753+341dup

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#.

59 SubSNP, 40 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80487489	Aug 21, 2014 (142)
2	HUMANGENOME_JCVI	ss96716616	Dec 05, 2013 (142)
3	PJP	ss294899318	May 09, 2011 (137)
4	PJP	ss294899319	May 09, 2011 (134)
5	1000GENOMES	ss1376159014	Aug 21, 2014 (142)
6	EVA_UK10K_ALSPAC	ss1708636123	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1708636137	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710713639	Apr 01, 2015 (144)
9	EVA_UK10K_TWINSUK	ss1710713641	Apr 01, 2015 (144)
10	EVA_UK10K_ALSPAC	ss1710713644	Apr 01, 2015 (144)
11	EVA_UK10K_ALSPAC	ss1710713646	Apr 01, 2015 (144)
12	SWEGEN	ss3014958206	Nov 08, 2017 (151)
13	URBANLAB	ss3650568280	Oct 12, 2018 (152)
14	EVA_DECODE	ss3699800613	Jul 13, 2019 (153)
15	EVA_DECODE	ss3699800615	Jul 13, 2019 (153)
16	EVA_DECODE	ss3699800616	Jul 13, 2019 (153)
17	EVA_DECODE	ss3699800617	Jul 13, 2019 (153)
18	EVA	ss3834706655	Apr 27, 2020 (154)
19	GNOMAD	ss4305677413	Apr 27, 2021 (155)
20	GNOMAD	ss4305677414	Apr 27, 2021 (155)
21	GNOMAD	ss4305677415	Apr 27, 2021 (155)
22	GNOMAD	ss4305677416	Apr 27, 2021 (155)
23	GNOMAD	ss4305677417	Apr 27, 2021 (155)
24	GNOMAD	ss4305677418	Apr 27, 2021 (155)
25	GNOMAD	ss4305677419	Apr 27, 2021 (155)
26	GNOMAD	ss4305677420	Apr 27, 2021 (155)
27	GNOMAD	ss4305677421	Apr 27, 2021 (155)
28	GNOMAD	ss4305677422	Apr 27, 2021 (155)
29	GNOMAD	ss4305677423	Apr 27, 2021 (155)
30	GNOMAD	ss4305677424	Apr 27, 2021 (155)
31	GNOMAD	ss4305677425	Apr 27, 2021 (155)
32	GNOMAD	ss4305677426	Apr 27, 2021 (155)
33	GNOMAD	ss4305677427	Apr 27, 2021 (155)
34	GNOMAD	ss4305677428	Apr 27, 2021 (155)
35	GNOMAD	ss4305677429	Apr 27, 2021 (155)
36	GNOMAD	ss4305677430	Apr 27, 2021 (155)
37	GNOMAD	ss4305677431	Apr 27, 2021 (155)
38	GNOMAD	ss4305677432	Apr 27, 2021 (155)
39	GNOMAD	ss4305677433	Apr 27, 2021 (155)
40	GNOMAD	ss4305677434	Apr 27, 2021 (155)
41	GNOMAD	ss4305677435	Apr 27, 2021 (155)
42	GNOMAD	ss4305677436	Apr 27, 2021 (155)
43	TOMMO_GENOMICS	ss5220822974	Apr 27, 2021 (155)
44	TOMMO_GENOMICS	ss5220822975	Apr 27, 2021 (155)
45	TOMMO_GENOMICS	ss5220822976	Apr 27, 2021 (155)
46	TOMMO_GENOMICS	ss5220822977	Apr 27, 2021 (155)
47	1000G_HIGH_COVERAGE	ss5301918206	Oct 16, 2022 (156)
48	HUGCELL_USP	ss5495167674	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5495167675	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5495167676	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5495167677	Oct 16, 2022 (156)
52	TOMMO_GENOMICS	ss5776193883	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5776193884	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5776193885	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5776193886	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5776193887	Oct 16, 2022 (156)
57	EVA	ss5846785795	Oct 16, 2022 (156)
58	EVA	ss5846785796	Oct 16, 2022 (156)
59	EVA	ss5980938341	Oct 16, 2022 (156)
60	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39145211 (NC_000016.9:85133404:T: 1691/3854) Row 39145212 (NC_000016.9:85133403:TTT: 867/3854) Row 39145213 (NC_000016.9:85133403::TTTT 715/3854)	-	Oct 12, 2018 (152)
61	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39145211 (NC_000016.9:85133404:T: 1691/3854) Row 39145212 (NC_000016.9:85133403:TTT: 867/3854) Row 39145213 (NC_000016.9:85133403::TTTT 715/3854)	-	Oct 12, 2018 (152)
62	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 39145211 (NC_000016.9:85133404:T: 1691/3854) Row 39145212 (NC_000016.9:85133403:TTT: 867/3854) Row 39145213 (NC_000016.9:85133403::TTTT 715/3854)	-	Oct 12, 2018 (152)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 497538433 (NC_000016.10:85099797::T 378/71810) Row 497538434 (NC_000016.10:85099797::TT 21/71768) Row 497538435 (NC_000016.10:85099797::TTT 32/71800)...	-	Apr 27, 2021 (155)
87	8.3KJPN Submission ignored due to conflicting rows: Row 78792281 (NC_000016.9:85133403:T: 3325/15942) Row 78792282 (NC_000016.9:85133403:TT: 2542/15942) Row 78792283 (NC_000016.9:85133403::T 20/15942)...	-	Apr 27, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 78792281 (NC_000016.9:85133403:T: 3325/15942) Row 78792282 (NC_000016.9:85133403:TT: 2542/15942) Row 78792283 (NC_000016.9:85133403::T 20/15942)...	-	Apr 27, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 78792281 (NC_000016.9:85133403:T: 3325/15942) Row 78792282 (NC_000016.9:85133403:TT: 2542/15942) Row 78792283 (NC_000016.9:85133403::T 20/15942)...	-	Apr 27, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 78792281 (NC_000016.9:85133403:T: 3325/15942) Row 78792282 (NC_000016.9:85133403:TT: 2542/15942) Row 78792283 (NC_000016.9:85133403::T 20/15942)...	-	Apr 27, 2021 (155)
91	14KJPN Submission ignored due to conflicting rows: Row 110030987 (NC_000016.10:85099797:TT: 4084/23906) Row 110030988 (NC_000016.10:85099797:T: 5142/23906) Row 110030989 (NC_000016.10:85099797::T 26/23906)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 110030987 (NC_000016.10:85099797:TT: 4084/23906) Row 110030988 (NC_000016.10:85099797:T: 5142/23906) Row 110030989 (NC_000016.10:85099797::T 26/23906)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 110030987 (NC_000016.10:85099797:TT: 4084/23906) Row 110030988 (NC_000016.10:85099797:T: 5142/23906) Row 110030989 (NC_000016.10:85099797::T 26/23906)...	-	Oct 16, 2022 (156)
94	14KJPN Submission ignored due to conflicting rows: Row 110030987 (NC_000016.10:85099797:TT: 4084/23906) Row 110030988 (NC_000016.10:85099797:T: 5142/23906) Row 110030989 (NC_000016.10:85099797::T 26/23906)...	-	Oct 16, 2022 (156)
95	14KJPN Submission ignored due to conflicting rows: Row 110030987 (NC_000016.10:85099797:TT: 4084/23906) Row 110030988 (NC_000016.10:85099797:T: 5142/23906) Row 110030989 (NC_000016.10:85099797::T 26/23906)...	-	Oct 16, 2022 (156)
96	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39145211 (NC_000016.9:85133404:T: 1558/3708) Row 39145212 (NC_000016.9:85133403:TTT: 810/3708) Row 39145213 (NC_000016.9:85133403::TTTT 768/3708)	-	Oct 12, 2018 (152)
97	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39145211 (NC_000016.9:85133404:T: 1558/3708) Row 39145212 (NC_000016.9:85133403:TTT: 810/3708) Row 39145213 (NC_000016.9:85133403::TTTT 768/3708)	-	Oct 12, 2018 (152)
98	UK 10K study - Twins Submission ignored due to conflicting rows: Row 39145211 (NC_000016.9:85133404:T: 1558/3708) Row 39145212 (NC_000016.9:85133403:TTT: 810/3708) Row 39145213 (NC_000016.9:85133403::TTTT 768/3708)	-	Oct 12, 2018 (152)
99	ALFA	NC_000016.10 - 85099798	Apr 27, 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)
rs71847404	May 11, 2012 (137)
rs71896514	May 11, 2012 (137)
rs148984344	May 11, 2012 (137)
rs398042274	Aug 21, 2014 (142)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4305677436	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4305677435	NC_000016.10:85099797:TTTTTTTTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4305677434	NC_000016.10:85099797:TTTTTTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4305677433	NC_000016.10:85099797:TTTTTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4305677432	NC_000016.10:85099797:TTTTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4305677431	NC_000016.10:85099797:TTTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3014958206	NC_000016.9:85133403:TTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4305677430	NC_000016.10:85099797:TTTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4305677429	NC_000016.10:85099797:TTTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4305677428, ss5495167677	NC_000016.10:85099797:TTTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1708636123, ss1708636137, ss5220822977, ss5846785796	NC_000016.9:85133403:TTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3699800613, ss4305677427, ss5495167675, ss5776193887	NC_000016.10:85099797:TTT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss80487489	NC_000016.8:83690926:TT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss5220822975, ss5846785795	NC_000016.9:85133403:TT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710713639, ss1710713644	NC_000016.9:85133404:TT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677426, ss5495167676, ss5776193883	NC_000016.10:85099797:TT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3699800615	NC_000016.10:85099798:TT:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss294899318	NC_000016.8:83690904:T:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss294899319	NC_000016.8:83690927:T:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3834706655, ss5220822974, ss5980938341	NC_000016.9:85133403:T:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1376159014	NC_000016.9:85133404:T:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3650568280, ss4305677425, ss5301918206, ss5495167674, ss5776193884	NC_000016.10:85099797:T:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3699800616	NC_000016.10:85099799:T:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss96716616	NT_010498.15:38747625:T:	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5220822976	NC_000016.9:85133403::T	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677413, ss5776193885	NC_000016.10:85099797::T	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677414, ss5776193886	NC_000016.10:85099797::TT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677415	NC_000016.10:85099797::TTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
	NC_000016.9:85133403::TTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss1710713641, ss1710713646	NC_000016.9:85133406::TTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677416	NC_000016.10:85099797::TTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3699800617	NC_000016.10:85099800::TTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677417	NC_000016.10:85099797::TTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677418	NC_000016.10:85099797::TTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677419	NC_000016.10:85099797::TTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677420	NC_000016.10:85099797::TTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677421	NC_000016.10:85099797::TTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677422	NC_000016.10:85099797::TTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677423	NC_000016.10:85099797::TTTTTTTTTTT… NC_000016.10:85099797::TTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4305677424	NC_000016.10:85099797::TTTTTTTTTTT… NC_000016.10:85099797::TTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
4252366263	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000016.10:85099797:TTTTTTTTTTTT… NC_000016.10:85099797:TTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs71386075

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

rs71386075