Name: rs773199651
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.

rs773199651

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:58290109-58290131 (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)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)₁₁ / dup(T)₂₃
Variation Type: Indel Insertion and Deletion
Frequency: dupT=0.3231 (2036/6302, ALFA)
(T)₂₃=0.00 (0/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: ZNF8 : Intron Variant
ZNF8-ERVK3-1 : 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	6302	TTTTTTTTTTTTTTTTTTTTTTT=0.6382	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.3231, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0113, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0211, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0022, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0016, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0025, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.617288	0.269492	0.11322	32
European	Sub	5440	TTTTTTTTTTTTTTTTTTTTTTT=0.5818	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.3735, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0131, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0243, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0026, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0018, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0029, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	0.552778	0.315079	0.132143	32
African	Sub	590	TTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	32	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	558	TTTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	42	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	34	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 1	Sub	22	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	100	TTTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	8	TTTTTTTTTTTTTTTTTTTTTTT=1.0	TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	100	TTTTTTTTTTTTTTTTTTTTTTT=0.95	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTTT=0.04, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.01, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	0.959184	0.020408	0.020408	12

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	6302	(T)₂₃=0.6382	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=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=0.0000, dupT=0.3231, dupTT=0.0211, dupTTT=0.0113, dup(T)₄=0.0016, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0022, dup(T)₈=0.0025
Allele Frequency Aggregator	European	Sub	5440	(T)₂₃=0.5818	del(T)₁₂=0.0000, del(T)₁₁=0.0000, del(T)₁₀=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=0.0000, dupT=0.3735, dupTT=0.0243, dupTTT=0.0131, dup(T)₄=0.0018, dup(T)₅=0.0000, dup(T)₆=0.0000, dup(T)₇=0.0026, dup(T)₈=0.0029
Allele Frequency Aggregator	African	Sub	590	(T)₂₃=1.000	del(T)₁₂=0.000, del(T)₁₁=0.000, del(T)₁₀=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, dup(T)₈=0.000
Allele Frequency Aggregator	Latin American 2	Sub	100	(T)₂₃=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=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, dup(T)₈=0.00
Allele Frequency Aggregator	Other	Sub	100	(T)₂₃=0.95	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=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=0.04, dupTT=0.01, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00
Allele Frequency Aggregator	Asian	Sub	42	(T)₂₃=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=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, dup(T)₈=0.00
Allele Frequency Aggregator	Latin American 1	Sub	22	(T)₂₃=1.00	del(T)₁₂=0.00, del(T)₁₁=0.00, del(T)₁₀=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, dup(T)₈=0.00
Allele Frequency Aggregator	South Asian	Sub	8	(T)₂₃=1.0	del(T)₁₂=0.0, del(T)₁₁=0.0, del(T)₁₀=0.0, del(T)₈=0.0, del(T)₇=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0, dup(T)₈=0.0
The Danish reference pan genome	Danish	Study-wide	40	(T)₂₃=0.00	del(T)₁₁=1.00

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 19	NC_000019.10:g.58290118_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290120_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290121_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290122_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290124_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290125_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290126_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290127_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290128_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290129_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290130_58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290131del
GRCh38.p14 chr 19	NC_000019.10:g.58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290130_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290129_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290128_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290127_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290126_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290125_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290124_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290123_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290121_58290131dup
GRCh38.p14 chr 19	NC_000019.10:g.58290109_58290131dup
GRCh37.p13 chr 19	NC_000019.9:g.58801484_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801486_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801487_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801488_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801490_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801491_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801492_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801493_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801494_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801495_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801496_58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801497del
GRCh37.p13 chr 19	NC_000019.9:g.58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801496_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801495_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801494_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801493_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801492_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801491_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801490_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801489_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801487_58801497dup
GRCh37.p13 chr 19	NC_000019.9:g.58801475_58801497dup

Gene: ZNF8, zinc finger protein 8 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF8 transcript	NM_021089.3:c.289+3913_28… NM_021089.3:c.289+3913_289+3926del	N/A	Intron Variant

Gene: ZNF8-ERVK3-1, ZNF8-ERVK3-1 readthrough (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
ZNF8-ERVK3-1 transcript	NR_144447.1:n.	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)₂₃=	del(T)₁₄	del(T)₁₂	del(T)₁₁	del(T)₁₀	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)₁₁	dup(T)₂₃
GRCh38.p14 chr 19	NC_000019.10:g.58290109_58290131=	NC_000019.10:g.58290118_58290131del	NC_000019.10:g.58290120_58290131del	NC_000019.10:g.58290121_58290131del	NC_000019.10:g.58290122_58290131del	NC_000019.10:g.58290124_58290131del	NC_000019.10:g.58290125_58290131del	NC_000019.10:g.58290126_58290131del	NC_000019.10:g.58290127_58290131del	NC_000019.10:g.58290128_58290131del	NC_000019.10:g.58290129_58290131del	NC_000019.10:g.58290130_58290131del	NC_000019.10:g.58290131del	NC_000019.10:g.58290131dup	NC_000019.10:g.58290130_58290131dup	NC_000019.10:g.58290129_58290131dup	NC_000019.10:g.58290128_58290131dup	NC_000019.10:g.58290127_58290131dup	NC_000019.10:g.58290126_58290131dup	NC_000019.10:g.58290125_58290131dup	NC_000019.10:g.58290124_58290131dup	NC_000019.10:g.58290123_58290131dup	NC_000019.10:g.58290121_58290131dup	NC_000019.10:g.58290109_58290131dup
GRCh37.p13 chr 19	NC_000019.9:g.58801475_58801497=	NC_000019.9:g.58801484_58801497del	NC_000019.9:g.58801486_58801497del	NC_000019.9:g.58801487_58801497del	NC_000019.9:g.58801488_58801497del	NC_000019.9:g.58801490_58801497del	NC_000019.9:g.58801491_58801497del	NC_000019.9:g.58801492_58801497del	NC_000019.9:g.58801493_58801497del	NC_000019.9:g.58801494_58801497del	NC_000019.9:g.58801495_58801497del	NC_000019.9:g.58801496_58801497del	NC_000019.9:g.58801497del	NC_000019.9:g.58801497dup	NC_000019.9:g.58801496_58801497dup	NC_000019.9:g.58801495_58801497dup	NC_000019.9:g.58801494_58801497dup	NC_000019.9:g.58801493_58801497dup	NC_000019.9:g.58801492_58801497dup	NC_000019.9:g.58801491_58801497dup	NC_000019.9:g.58801490_58801497dup	NC_000019.9:g.58801489_58801497dup	NC_000019.9:g.58801487_58801497dup	NC_000019.9:g.58801475_58801497dup
ZNF8 transcript	NM_021089.2:c.289+3904=	NM_021089.2:c.289+3913_289+3926del	NM_021089.2:c.289+3915_289+3926del	NM_021089.2:c.289+3916_289+3926del	NM_021089.2:c.289+3917_289+3926del	NM_021089.2:c.289+3919_289+3926del	NM_021089.2:c.289+3920_289+3926del	NM_021089.2:c.289+3921_289+3926del	NM_021089.2:c.289+3922_289+3926del	NM_021089.2:c.289+3923_289+3926del	NM_021089.2:c.289+3924_289+3926del	NM_021089.2:c.289+3925_289+3926del	NM_021089.2:c.289+3926del	NM_021089.2:c.289+3926dup	NM_021089.2:c.289+3925_289+3926dup	NM_021089.2:c.289+3924_289+3926dup	NM_021089.2:c.289+3923_289+3926dup	NM_021089.2:c.289+3922_289+3926dup	NM_021089.2:c.289+3921_289+3926dup	NM_021089.2:c.289+3920_289+3926dup	NM_021089.2:c.289+3919_289+3926dup	NM_021089.2:c.289+3918_289+3926dup	NM_021089.2:c.289+3916_289+3926dup	NM_021089.2:c.289+3904_289+3926dup
ZNF8 transcript	NM_021089.3:c.289+3904=	NM_021089.3:c.289+3913_289+3926del	NM_021089.3:c.289+3915_289+3926del	NM_021089.3:c.289+3916_289+3926del	NM_021089.3:c.289+3917_289+3926del	NM_021089.3:c.289+3919_289+3926del	NM_021089.3:c.289+3920_289+3926del	NM_021089.3:c.289+3921_289+3926del	NM_021089.3:c.289+3922_289+3926del	NM_021089.3:c.289+3923_289+3926del	NM_021089.3:c.289+3924_289+3926del	NM_021089.3:c.289+3925_289+3926del	NM_021089.3:c.289+3926del	NM_021089.3:c.289+3926dup	NM_021089.3:c.289+3925_289+3926dup	NM_021089.3:c.289+3924_289+3926dup	NM_021089.3:c.289+3923_289+3926dup	NM_021089.3:c.289+3922_289+3926dup	NM_021089.3:c.289+3921_289+3926dup	NM_021089.3:c.289+3920_289+3926dup	NM_021089.3:c.289+3919_289+3926dup	NM_021089.3:c.289+3918_289+3926dup	NM_021089.3:c.289+3916_289+3926dup	NM_021089.3:c.289+3904_289+3926dup
ZNF8 transcript variant X1	XM_005259201.1:c.289+3904=	XM_005259201.1:c.289+3913_289+3926del	XM_005259201.1:c.289+3915_289+3926del	XM_005259201.1:c.289+3916_289+3926del	XM_005259201.1:c.289+3917_289+3926del	XM_005259201.1:c.289+3919_289+3926del	XM_005259201.1:c.289+3920_289+3926del	XM_005259201.1:c.289+3921_289+3926del	XM_005259201.1:c.289+3922_289+3926del	XM_005259201.1:c.289+3923_289+3926del	XM_005259201.1:c.289+3924_289+3926del	XM_005259201.1:c.289+3925_289+3926del	XM_005259201.1:c.289+3926del	XM_005259201.1:c.289+3926dup	XM_005259201.1:c.289+3925_289+3926dup	XM_005259201.1:c.289+3924_289+3926dup	XM_005259201.1:c.289+3923_289+3926dup	XM_005259201.1:c.289+3922_289+3926dup	XM_005259201.1:c.289+3921_289+3926dup	XM_005259201.1:c.289+3920_289+3926dup	XM_005259201.1:c.289+3919_289+3926dup	XM_005259201.1:c.289+3918_289+3926dup	XM_005259201.1:c.289+3916_289+3926dup	XM_005259201.1:c.289+3904_289+3926dup

Submissions tab displays variations originally submitted to dbSNP, now supporting this RefSNP cluster (rs). We display Submitter handle, Submission identifier, Date and Build number, when the submission appeared for the first time. Direct submissions to dbSNP have Submission ID in the form of an ss-prefixed number (ss#). Other supporting variations are listed in the table without ss#.

41 SubSNP, 31 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	PJP	ss294969164	Oct 12, 2018 (152)
2	EVA_GENOME_DK	ss1577606587	Apr 01, 2015 (144)
3	SWEGEN	ss3017738948	Nov 08, 2017 (151)
4	SWEGEN	ss3017738949	Nov 08, 2017 (151)
5	PACBIO	ss3793479661	Jul 13, 2019 (153)
6	PACBIO	ss3798366797	Jul 13, 2019 (153)
7	GNOMAD	ss4333769398	Apr 27, 2021 (155)
8	GNOMAD	ss4333769399	Apr 27, 2021 (155)
9	GNOMAD	ss4333769400	Apr 27, 2021 (155)
10	GNOMAD	ss4333769401	Apr 27, 2021 (155)
11	GNOMAD	ss4333769402	Apr 27, 2021 (155)
12	GNOMAD	ss4333769403	Apr 27, 2021 (155)
13	GNOMAD	ss4333769404	Apr 27, 2021 (155)
14	GNOMAD	ss4333769405	Apr 27, 2021 (155)
15	GNOMAD	ss4333769406	Apr 27, 2021 (155)
16	GNOMAD	ss4333769408	Apr 27, 2021 (155)
17	GNOMAD	ss4333769409	Apr 27, 2021 (155)
18	GNOMAD	ss4333769410	Apr 27, 2021 (155)
19	GNOMAD	ss4333769411	Apr 27, 2021 (155)
20	GNOMAD	ss4333769412	Apr 27, 2021 (155)
21	GNOMAD	ss4333769413	Apr 27, 2021 (155)
22	GNOMAD	ss4333769414	Apr 27, 2021 (155)
23	GNOMAD	ss4333769415	Apr 27, 2021 (155)
24	GNOMAD	ss4333769416	Apr 27, 2021 (155)
25	GNOMAD	ss4333769417	Apr 27, 2021 (155)
26	GNOMAD	ss4333769418	Apr 27, 2021 (155)
27	GNOMAD	ss4333769419	Apr 27, 2021 (155)
28	TOMMO_GENOMICS	ss5228491389	Apr 27, 2021 (155)
29	TOMMO_GENOMICS	ss5228491390	Apr 27, 2021 (155)
30	TOMMO_GENOMICS	ss5228491391	Apr 27, 2021 (155)
31	TOMMO_GENOMICS	ss5228491392	Apr 27, 2021 (155)
32	1000G_HIGH_COVERAGE	ss5307810453	Oct 16, 2022 (156)
33	1000G_HIGH_COVERAGE	ss5307810454	Oct 16, 2022 (156)
34	1000G_HIGH_COVERAGE	ss5307810455	Oct 16, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5307810457	Oct 16, 2022 (156)
36	HUGCELL_USP	ss5500238061	Oct 16, 2022 (156)
37	HUGCELL_USP	ss5500238062	Oct 16, 2022 (156)
38	TOMMO_GENOMICS	ss5787376229	Oct 16, 2022 (156)
39	TOMMO_GENOMICS	ss5787376230	Oct 16, 2022 (156)
40	TOMMO_GENOMICS	ss5787376232	Oct 16, 2022 (156)
41	TOMMO_GENOMICS	ss5787376233	Oct 16, 2022 (156)
42	The Danish reference pan genome	NC_000019.9 - 58801475	Apr 27, 2020 (154)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 544296765 (NC_000019.10:58290108::TTT 1137/69314) Row 544296766 (NC_000019.10:58290108::TTTT 329/69374) Row 544296767 (NC_000019.10:58290108::TTTTT 397/69382)...	-	Apr 27, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 86460696 (NC_000019.9:58801474::T 5769/16260) Row 86460697 (NC_000019.9:58801474::TT 313/16260) Row 86460698 (NC_000019.9:58801474:T: 64/16260)...	-	Apr 27, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 86460696 (NC_000019.9:58801474::T 5769/16260) Row 86460697 (NC_000019.9:58801474::TT 313/16260) Row 86460698 (NC_000019.9:58801474:T: 64/16260)...	-	Apr 27, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 86460696 (NC_000019.9:58801474::T 5769/16260) Row 86460697 (NC_000019.9:58801474::TT 313/16260) Row 86460698 (NC_000019.9:58801474:T: 64/16260)...	-	Apr 27, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 86460696 (NC_000019.9:58801474::T 5769/16260) Row 86460697 (NC_000019.9:58801474::TT 313/16260) Row 86460698 (NC_000019.9:58801474:T: 64/16260)...	-	Apr 27, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 121213333 (NC_000019.10:58290108::T 8680/25200) Row 121213334 (NC_000019.10:58290108::TT 376/25200) Row 121213336 (NC_000019.10:58290108:TTTTTTTTTT: 6/25200)...	-	Oct 16, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 121213333 (NC_000019.10:58290108::T 8680/25200) Row 121213334 (NC_000019.10:58290108::TT 376/25200) Row 121213336 (NC_000019.10:58290108:TTTTTTTTTT: 6/25200)...	-	Oct 16, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 121213333 (NC_000019.10:58290108::T 8680/25200) Row 121213334 (NC_000019.10:58290108::TT 376/25200) Row 121213336 (NC_000019.10:58290108:TTTTTTTTTT: 6/25200)...	-	Oct 16, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 121213333 (NC_000019.10:58290108::T 8680/25200) Row 121213334 (NC_000019.10:58290108::TT 376/25200) Row 121213336 (NC_000019.10:58290108:TTTTTTTTTT: 6/25200)...	-	Oct 16, 2022 (156)
72	ALFA	NC_000019.10 - 58290109	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4333769419	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
ss4333769418	NC_000019.10:58290108:TTTTTTTTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
52917, ss1577606587, ss5228491392	NC_000019.9:58801474:TTTTTTTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4333769417	NC_000019.10:58290108:TTTTTTTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4333769416, ss5787376232	NC_000019.10:58290108:TTTTTTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4333769415	NC_000019.10:58290108:TTTTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4333769414	NC_000019.10:58290108:TTTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4333769413	NC_000019.10:58290108:TTTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4333769412	NC_000019.10:58290108:TTTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4333769411	NC_000019.10:58290108:TTTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4333769410	NC_000019.10:58290108:TTT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4333769409	NC_000019.10:58290108:TT:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5228491391	NC_000019.9:58801474:T:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769408, ss5500238062, ss5787376233	NC_000019.10:58290108:T:	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss294969164	NC_000019.8:63493287::T	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3017738948, ss3793479661, ss3798366797, ss5228491389	NC_000019.9:58801474::T	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5500238061, ss5787376229	NC_000019.10:58290108::T	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3017738949, ss5228491390	NC_000019.9:58801474::TT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5307810454, ss5787376230	NC_000019.10:58290108::TT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769398, ss5307810453	NC_000019.10:58290108::TTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769399, ss5307810457	NC_000019.10:58290108::TTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769400, ss5307810455	NC_000019.10:58290108::TTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769401	NC_000019.10:58290108::TTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769402	NC_000019.10:58290108::TTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769403	NC_000019.10:58290108::TTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
8983611334	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769404	NC_000019.10:58290108::TTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769405	NC_000019.10:58290108::TTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4333769406	NC_000019.10:58290108::TTTTTTTTTTT… NC_000019.10:58290108::TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:58290108:TTTTTTTTTTTT… NC_000019.10:58290108:TTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(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 rs773199651

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

rs773199651