Name: rs77550533
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.

rs77550533

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr19:48657617-48657638 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(T)₁₂ / del(T)₁₁ / del(T)₁₀ / d…
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)₁₂ / dup(T)₁₃ / dup(T)₁₄ / ins(T)₁₄C(T)₂₆ / dup(T)₁₆ / dup(T)₁₇ / dup(T)₁₈ / dup(T)₂₀ / dup(T)₂₂ / ins(T)₂₃
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₁₂=0.0000 (0/3852, ALFA)
del(T)₁₁=0.0000 (0/3852, ALFA)
del(T)₁₀=0.0000 (0/3852, ALFA) (+ 14 more)
del(T)₉=0.0000 (0/3852, ALFA)
del(T)₈=0.0000 (0/3852, ALFA)
del(T)₇=0.0000 (0/3852, ALFA)
del(T)₆=0.0000 (0/3852, ALFA)
del(T)₅=0.0000 (0/3852, ALFA)
del(T)₄=0.0000 (0/3852, ALFA)
delTTT=0.0000 (0/3852, ALFA)
delTT=0.0000 (0/3852, ALFA)
delT=0.0000 (0/3852, ALFA)
dupT=0.0000 (0/3852, ALFA)
dupTT=0.0000 (0/3852, ALFA)
dupTTT=0.0000 (0/3852, ALFA)
dup(T)₄=0.0000 (0/3852, ALFA)
dup(T)₅=0.0000 (0/3852, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: SEC1P : Intron Variant
Publications: 0 citations
Genomic View: See rs on genome

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

Release Version: 20231103111315

Population	Group	Sample Size	Ref Allele	Alt Allele	Ref HMOZ	HWEP
Total	Global	3852	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=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=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
European	Sub	2558	TTTTTTTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTT=0.0000, TTTTTTTTTTT=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=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	680	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African Others	Sub	32	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
African American	Sub	648	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Asian	Sub	60	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
East Asian	Sub	44	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	16	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	42	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 2	Sub	326	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	42	TTTTTTTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTT=0.00, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	144	TTTTTTTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTT=0.000, TTTTTTTTTTT=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, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A

Frequency tab displays a table of the reference and alternate allele frequencies reported by various studies and populations. Table lines, where Population="Global" refer to the entire study population, whereas lines, where Group="Sub", refer to a study-specific population subgroupings (i.e. AFR, CAU, etc.), if available. Frequency for the alternate allele (Alt Allele) is a ratio of samples observed-to-total, where the numerator (observed samples) is the number of chromosomes in the study with the minor allele present (found in "Sample size", where Group="Sub"), and the denominator (total samples) is the total number of all chromosomes in the study for the variant (found in "Sample size", where Group="Study-wide" and Population="Global").

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	3852	(T)₂₂=1.0000	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=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	European	Sub	2558	(T)₂₂=1.0000	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=0.0000, dupT=0.0000, dupTT=0.0000, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₅=0.0000
Allele Frequency Aggregator	African	Sub	680	(T)₂₂=1.000	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
Allele Frequency Aggregator	Latin American 2	Sub	326	(T)₂₂=1.000	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
Allele Frequency Aggregator	Other	Sub	144	(T)₂₂=1.000	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
Allele Frequency Aggregator	Asian	Sub	60	(T)₂₂=1.00	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
Allele Frequency Aggregator	Latin American 1	Sub	42	(T)₂₂=1.00	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
Allele Frequency Aggregator	South Asian	Sub	42	(T)₂₂=1.00	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

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.48657627_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657628_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657629_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657630_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657631_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657632_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657633_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657634_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657635_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657636_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657637_48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657638del
GRCh38.p14 chr 19	NC_000019.10:g.48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657637_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657636_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657635_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657634_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657633_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657632_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657631_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657630_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657629_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657627_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657626_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657625_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657617_48657638T[36]CTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 19	NC_000019.10:g.48657623_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657622_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657621_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657619_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657617_48657638dup
GRCh38.p14 chr 19	NC_000019.10:g.48657638_48657639insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.49160884_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160885_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160886_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160887_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160888_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160889_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160890_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160891_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160892_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160893_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160894_49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160895del
GRCh37.p13 chr 19	NC_000019.9:g.49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160894_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160893_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160892_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160891_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160890_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160889_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160888_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160887_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160886_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160884_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160883_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160882_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160874_49160895T[36]CTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 19	NC_000019.9:g.49160880_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160879_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160878_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160876_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160874_49160895dup
GRCh37.p13 chr 19	NC_000019.9:g.49160895_49160896insTTTTTTTTTTTTTTTTTTTTTTT

Gene: SEC1P, secretory blood group 1, pseudogene (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
SEC1P transcript	NR_004401.2: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)₂₂=	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)₁₂	dup(T)₁₃	dup(T)₁₄	ins(T)₁₄C(T)₂₆	dup(T)₁₆	dup(T)₁₇	dup(T)₁₈	dup(T)₂₀	dup(T)₂₂	ins(T)₂₃
GRCh38.p14 chr 19	NC_000019.10:g.48657617_48657638=	NC_000019.10:g.48657627_48657638del	NC_000019.10:g.48657628_48657638del	NC_000019.10:g.48657629_48657638del	NC_000019.10:g.48657630_48657638del	NC_000019.10:g.48657631_48657638del	NC_000019.10:g.48657632_48657638del	NC_000019.10:g.48657633_48657638del	NC_000019.10:g.48657634_48657638del	NC_000019.10:g.48657635_48657638del	NC_000019.10:g.48657636_48657638del	NC_000019.10:g.48657637_48657638del	NC_000019.10:g.48657638del	NC_000019.10:g.48657638dup	NC_000019.10:g.48657637_48657638dup	NC_000019.10:g.48657636_48657638dup	NC_000019.10:g.48657635_48657638dup	NC_000019.10:g.48657634_48657638dup	NC_000019.10:g.48657633_48657638dup	NC_000019.10:g.48657632_48657638dup	NC_000019.10:g.48657631_48657638dup	NC_000019.10:g.48657630_48657638dup	NC_000019.10:g.48657629_48657638dup	NC_000019.10:g.48657627_48657638dup	NC_000019.10:g.48657626_48657638dup	NC_000019.10:g.48657625_48657638dup	NC_000019.10:g.48657617_48657638T[36]CTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000019.10:g.48657623_48657638dup	NC_000019.10:g.48657622_48657638dup	NC_000019.10:g.48657621_48657638dup	NC_000019.10:g.48657619_48657638dup	NC_000019.10:g.48657617_48657638dup	NC_000019.10:g.48657638_48657639insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 19	NC_000019.9:g.49160874_49160895=	NC_000019.9:g.49160884_49160895del	NC_000019.9:g.49160885_49160895del	NC_000019.9:g.49160886_49160895del	NC_000019.9:g.49160887_49160895del	NC_000019.9:g.49160888_49160895del	NC_000019.9:g.49160889_49160895del	NC_000019.9:g.49160890_49160895del	NC_000019.9:g.49160891_49160895del	NC_000019.9:g.49160892_49160895del	NC_000019.9:g.49160893_49160895del	NC_000019.9:g.49160894_49160895del	NC_000019.9:g.49160895del	NC_000019.9:g.49160895dup	NC_000019.9:g.49160894_49160895dup	NC_000019.9:g.49160893_49160895dup	NC_000019.9:g.49160892_49160895dup	NC_000019.9:g.49160891_49160895dup	NC_000019.9:g.49160890_49160895dup	NC_000019.9:g.49160889_49160895dup	NC_000019.9:g.49160888_49160895dup	NC_000019.9:g.49160887_49160895dup	NC_000019.9:g.49160886_49160895dup	NC_000019.9:g.49160884_49160895dup	NC_000019.9:g.49160883_49160895dup	NC_000019.9:g.49160882_49160895dup	NC_000019.9:g.49160874_49160895T[36]CTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000019.9:g.49160880_49160895dup	NC_000019.9:g.49160879_49160895dup	NC_000019.9:g.49160878_49160895dup	NC_000019.9:g.49160876_49160895dup	NC_000019.9:g.49160874_49160895dup	NC_000019.9:g.49160895_49160896insTTTTTTTTTTTTTTTTTTTTTTT

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#.

56 SubSNP, 38 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81959832	Aug 21, 2014 (142)
2	BCMHGSC_JDW	ss103618119	Dec 01, 2009 (131)
3	EVA_DECODE	ss3702906145	Jul 13, 2019 (153)
4	EVA_DECODE	ss3702906146	Jul 13, 2019 (153)
5	EVA_DECODE	ss3702906147	Jul 13, 2019 (153)
6	EVA_DECODE	ss3702906148	Jul 13, 2019 (153)
7	EVA_DECODE	ss3702906149	Jul 13, 2019 (153)
8	EVA_DECODE	ss3702906150	Jul 13, 2019 (153)
9	EVA_DECODE	ss3702906153	Jul 13, 2019 (153)
10	PACBIO	ss3793457165	Jul 13, 2019 (153)
11	PACBIO	ss3793457166	Jul 13, 2019 (153)
12	PACBIO	ss3798344043	Jul 13, 2019 (153)
13	PACBIO	ss3798344044	Jul 13, 2019 (153)
14	EVA	ss3835496600	Apr 27, 2020 (154)
15	KOGIC	ss3981507575	Apr 27, 2020 (154)
16	KOGIC	ss3981507576	Apr 27, 2020 (154)
17	KOGIC	ss3981507577	Apr 27, 2020 (154)
18	GNOMAD	ss4332444795	Apr 26, 2021 (155)
19	GNOMAD	ss4332444796	Apr 26, 2021 (155)
20	GNOMAD	ss4332444797	Apr 26, 2021 (155)
21	GNOMAD	ss4332444798	Apr 26, 2021 (155)
22	GNOMAD	ss4332444799	Apr 26, 2021 (155)
23	GNOMAD	ss4332444800	Apr 26, 2021 (155)
24	GNOMAD	ss4332444801	Apr 26, 2021 (155)
25	GNOMAD	ss4332444802	Apr 26, 2021 (155)
26	GNOMAD	ss4332444803	Apr 26, 2021 (155)
27	GNOMAD	ss4332444804	Apr 26, 2021 (155)
28	GNOMAD	ss4332444805	Apr 26, 2021 (155)
29	GNOMAD	ss4332444806	Apr 26, 2021 (155)
30	GNOMAD	ss4332444807	Apr 26, 2021 (155)
31	GNOMAD	ss4332444808	Apr 26, 2021 (155)
32	GNOMAD	ss4332444809	Apr 26, 2021 (155)
33	GNOMAD	ss4332444810	Apr 26, 2021 (155)
34	GNOMAD	ss4332444811	Apr 26, 2021 (155)
35	GNOMAD	ss4332444812	Apr 26, 2021 (155)
36	GNOMAD	ss4332444813	Apr 26, 2021 (155)
37	GNOMAD	ss4332444814	Apr 26, 2021 (155)
38	GNOMAD	ss4332444815	Apr 26, 2021 (155)
39	GNOMAD	ss4332444816	Apr 26, 2021 (155)
40	GNOMAD	ss4332444817	Apr 26, 2021 (155)
41	GNOMAD	ss4332444818	Apr 26, 2021 (155)
42	GNOMAD	ss4332444819	Apr 26, 2021 (155)
43	GNOMAD	ss4332444820	Apr 26, 2021 (155)
44	GNOMAD	ss4332444821	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5228096156	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5228096157	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5228096158	Apr 26, 2021 (155)
48	1000G_HIGH_COVERAGE	ss5307505354	Oct 16, 2022 (156)
49	HUGCELL_USP	ss5499984716	Oct 16, 2022 (156)
50	HUGCELL_USP	ss5499984717	Oct 16, 2022 (156)
51	HUGCELL_USP	ss5499984718	Oct 16, 2022 (156)
52	HUGCELL_USP	ss5499984719	Oct 16, 2022 (156)
53	TOMMO_GENOMICS	ss5786843353	Oct 16, 2022 (156)
54	TOMMO_GENOMICS	ss5786843354	Oct 16, 2022 (156)
55	TOMMO_GENOMICS	ss5786843355	Oct 16, 2022 (156)
56	TOMMO_GENOMICS	ss5786843356	Oct 16, 2022 (156)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
63	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
64	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
65	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 542041443 (NC_000019.10:48657616::T 1971/79198) Row 542041444 (NC_000019.10:48657616::TT 153/79142) Row 542041445 (NC_000019.10:48657616::TTT 184/79192)...	-	Apr 26, 2021 (155)
84	Korean Genome Project Submission ignored due to conflicting rows: Row 37885576 (NC_000019.10:48657617:TT: 225/1814) Row 37885577 (NC_000019.10:48657616:TTT: 28/1814) Row 37885578 (NC_000019.10:48657618:T: 312/1814)	-	Apr 27, 2020 (154)
85	Korean Genome Project Submission ignored due to conflicting rows: Row 37885576 (NC_000019.10:48657617:TT: 225/1814) Row 37885577 (NC_000019.10:48657616:TTT: 28/1814) Row 37885578 (NC_000019.10:48657618:T: 312/1814)	-	Apr 27, 2020 (154)
86	Korean Genome Project Submission ignored due to conflicting rows: Row 37885576 (NC_000019.10:48657617:TT: 225/1814) Row 37885577 (NC_000019.10:48657616:TTT: 28/1814) Row 37885578 (NC_000019.10:48657618:T: 312/1814)	-	Apr 27, 2020 (154)
87	8.3KJPN Submission ignored due to conflicting rows: Row 86065463 (NC_000019.9:49160873:T: 1907/15224) Row 86065464 (NC_000019.9:49160873::T 74/15224) Row 86065465 (NC_000019.9:49160873:TT: 999/15224)	-	Apr 26, 2021 (155)
88	8.3KJPN Submission ignored due to conflicting rows: Row 86065463 (NC_000019.9:49160873:T: 1907/15224) Row 86065464 (NC_000019.9:49160873::T 74/15224) Row 86065465 (NC_000019.9:49160873:TT: 999/15224)	-	Apr 26, 2021 (155)
89	8.3KJPN Submission ignored due to conflicting rows: Row 86065463 (NC_000019.9:49160873:T: 1907/15224) Row 86065464 (NC_000019.9:49160873::T 74/15224) Row 86065465 (NC_000019.9:49160873:TT: 999/15224)	-	Apr 26, 2021 (155)
90	14KJPN Submission ignored due to conflicting rows: Row 120680457 (NC_000019.10:48657616:T: 3244/26168) Row 120680458 (NC_000019.10:48657616:TTT: 109/26168) Row 120680459 (NC_000019.10:48657616:TT: 1797/26168)...	-	Oct 16, 2022 (156)
91	14KJPN Submission ignored due to conflicting rows: Row 120680457 (NC_000019.10:48657616:T: 3244/26168) Row 120680458 (NC_000019.10:48657616:TTT: 109/26168) Row 120680459 (NC_000019.10:48657616:TT: 1797/26168)...	-	Oct 16, 2022 (156)
92	14KJPN Submission ignored due to conflicting rows: Row 120680457 (NC_000019.10:48657616:T: 3244/26168) Row 120680458 (NC_000019.10:48657616:TTT: 109/26168) Row 120680459 (NC_000019.10:48657616:TT: 1797/26168)...	-	Oct 16, 2022 (156)
93	14KJPN Submission ignored due to conflicting rows: Row 120680457 (NC_000019.10:48657616:T: 3244/26168) Row 120680458 (NC_000019.10:48657616:TTT: 109/26168) Row 120680459 (NC_000019.10:48657616:TT: 1797/26168)...	-	Oct 16, 2022 (156)
94	ALFA	NC_000019.10 - 48657617	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)
rs58212894	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4332444821	NC_000019.10:48657616:TTTTTTTTTTTT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4332444820	NC_000019.10:48657616:TTTTTTT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4332444819, ss5499984719	NC_000019.10:48657616:TTTTT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4332444818	NC_000019.10:48657616:TTTT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss103618119	NT_011109.16:21429109:TTTT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3981507576, ss4332444817, ss5307505354, ss5786843354	NC_000019.10:48657616:TTT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss81959832	NC_000019.8:53852705:TT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3793457165, ss3798344043, ss5228096158	NC_000019.9:49160873:TT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3702906145, ss4332444816, ss5499984717, ss5786843355	NC_000019.10:48657616:TT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3981507575	NC_000019.10:48657617:TT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3793457166, ss3798344044, ss3835496600, ss5228096156	NC_000019.9:49160873:T:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444815, ss5499984716, ss5786843353	NC_000019.10:48657616:T:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3702906146	NC_000019.10:48657617:T:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3981507577	NC_000019.10:48657618:T:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss5228096157	NC_000019.9:49160873::T	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444795, ss5499984718, ss5786843356	NC_000019.10:48657616::T	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702906147, ss3702906153	NC_000019.10:48657618::T	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444796	NC_000019.10:48657616::TT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702906148	NC_000019.10:48657618::TT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444797	NC_000019.10:48657616::TTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702906149	NC_000019.10:48657618::TTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444798	NC_000019.10:48657616::TTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3702906150	NC_000019.10:48657618::TTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444799	NC_000019.10:48657616::TTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
7571315129	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444800	NC_000019.10:48657616::TTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444801	NC_000019.10:48657616::TTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444802	NC_000019.10:48657616::TTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444803	NC_000019.10:48657616::TTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444804	NC_000019.10:48657616::TTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444805	NC_000019.10:48657616::TTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444806	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444807	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444814	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444808	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444809	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444810	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444811	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444812	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4332444813	NC_000019.10:48657616::TTTTTTTTTTT… NC_000019.10:48657616::TTTTTTTTTTTTTTTTTTTTTTT	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3295095863	NC_000019.10:48657616:TTTTTTTTTTT:	NC_000019.10:48657616:TTTTTTTTTTTT… NC_000019.10:48657616:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT

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

No publications for rs77550533

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.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs77550533