Name: rs61139169
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.

rs61139169

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr11:74217542-74217563 (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(A)₁₄ / del(A)₁₃ / del(A)₁₂ / d…
del(A)₁₄ / del(A)₁₃ / del(A)₁₂ / del(A)₁₁ / del(A)₁₀ / del(A)₉ / del(A)₈ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₁₀ / dup(A)₁₄ / dup(A)₁₈ / ins(A)₂₄ / ins(A)₂₅ / ins(A)₂₆
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₄=0.0000 (0/1506, ALFA)
del(A)₁₃=0.0000 (0/1506, ALFA)
del(A)₁₂=0.0000 (0/1506, ALFA) (+ 15 more)
del(A)₁₁=0.0000 (0/1506, ALFA)
del(A)₁₀=0.0000 (0/1506, ALFA)
del(A)₉=0.0000 (0/1506, ALFA)
del(A)₈=0.0000 (0/1506, ALFA)
del(A)₇=0.0000 (0/1506, ALFA)
del(A)₆=0.0000 (0/1506, ALFA)
del(A)₅=0.0000 (0/1506, ALFA)
del(A)₄=0.0000 (0/1506, ALFA)
delAAA=0.0000 (0/1506, ALFA)
delAA=0.0000 (0/1506, ALFA)
delA=0.0000 (0/1506, ALFA)
dupA=0.0000 (0/1506, ALFA)
dupAA=0.0000 (0/1506, ALFA)
dup(A)₇=0.0000 (0/1506, ALFA)
delA=0.42 (17/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: PPME1 : 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	1506	AAAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAA=0.0000, AAAAAAAAA=0.0000, AAAAAAAAAA=0.0000, AAAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	0.0	0.0	N/A
European	Sub	912	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African	Sub	436	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
African Others	Sub	18	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
African American	Sub	418	AAAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAA=0.000, AAAAAAAAA=0.000, AAAAAAAAAA=0.000, AAAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	0.0	0.0	N/A
Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	4	AAAAAAAAAAAAAAAAAAAAAA=1.0	AAAAAAAA=0.0, AAAAAAAAA=0.0, AAAAAAAAAA=0.0, AAAAAAAAAAA=0.0, AAAAAAAAAAAA=0.0, AAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAA=0.0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	AAAAAAAAAAAAAAAAAAAAAA=0	AAAAAAAA=0, AAAAAAAAA=0, AAAAAAAAAA=0, AAAAAAAAAAA=0, AAAAAAAAAAAA=0, AAAAAAAAAAAAA=0, AAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAA=0, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0	0	0	0	N/A
Latin American 1	Sub	24	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	62	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
South Asian	Sub	14	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	N/A
Other	Sub	54	AAAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAA=0.00, AAAAAAAAA=0.00, AAAAAAAAAA=0.00, AAAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	0.0	0.0	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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	1506	(A)₂₂=1.0000	del(A)₁₄=0.0000, del(A)₁₃=0.0000, del(A)₁₂=0.0000, del(A)₁₁=0.0000, del(A)₁₀=0.0000, del(A)₉=0.0000, del(A)₈=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dup(A)₇=0.0000
Allele Frequency Aggregator	European	Sub	912	(A)₂₂=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	African	Sub	436	(A)₂₂=1.000	del(A)₁₄=0.000, del(A)₁₃=0.000, del(A)₁₂=0.000, del(A)₁₁=0.000, del(A)₁₀=0.000, del(A)₉=0.000, del(A)₈=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dup(A)₇=0.000
Allele Frequency Aggregator	Latin American 2	Sub	62	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Other	Sub	54	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Latin American 1	Sub	24	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	South Asian	Sub	14	(A)₂₂=1.00	del(A)₁₄=0.00, del(A)₁₃=0.00, del(A)₁₂=0.00, del(A)₁₁=0.00, del(A)₁₀=0.00, del(A)₉=0.00, del(A)₈=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dup(A)₇=0.00
Allele Frequency Aggregator	Asian	Sub	4	(A)₂₂=1.0	del(A)₁₄=0.0, del(A)₁₃=0.0, del(A)₁₂=0.0, del(A)₁₁=0.0, del(A)₁₀=0.0, del(A)₉=0.0, del(A)₈=0.0, del(A)₇=0.0, del(A)₆=0.0, del(A)₅=0.0, del(A)₄=0.0, delAAA=0.0, delAA=0.0, delA=0.0, dupA=0.0, dupAA=0.0, dup(A)₇=0.0
The Danish reference pan genome	Danish	Study-wide	40	(A)₂₂=0.57	delA=0.42

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 11	NC_000011.10:g.74217550_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217551_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217552_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217553_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217554_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217555_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217556_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217557_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217558_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217559_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217560_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217561_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217562_74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217563del
GRCh38.p14 chr 11	NC_000011.10:g.74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217562_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217561_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217560_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217559_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217558_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217557_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217556_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217554_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217550_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217546_74217563dup
GRCh38.p14 chr 11	NC_000011.10:g.74217563_74217564insAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 11	NC_000011.10:g.74217563_74217564insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 11	NC_000011.10:g.74217563_74217564insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.73928595_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928596_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928597_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928598_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928599_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928600_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928601_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928602_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928603_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928604_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928605_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928606_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928607_73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928608del
GRCh37.p13 chr 11	NC_000011.9:g.73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928607_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928606_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928605_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928604_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928603_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928602_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928601_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928599_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928595_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928591_73928608dup
GRCh37.p13 chr 11	NC_000011.9:g.73928608_73928609insAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.73928608_73928609insAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.73928608_73928609insAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: PPME1, protein phosphatase methylesterase 1 (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
PPME1 transcript variant 2	NM_001271593.2:c.289-4762… NM_001271593.2:c.289-4762_289-4749del	N/A	Intron Variant
PPME1 transcript variant 1	NM_016147.3:c.289-4762_28… NM_016147.3:c.289-4762_289-4749del	N/A	Intron Variant
PPME1 transcript variant X2	XM_017017913.3:c.289-4762… XM_017017913.3:c.289-4762_289-4749del	N/A	Intron Variant
PPME1 transcript variant X1	XM_047427116.1:c.289-4762… XM_047427116.1:c.289-4762_289-4749del	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	(A)₂₂=	del(A)₁₄	del(A)₁₃	del(A)₁₂	del(A)₁₁	del(A)₁₀	del(A)₉	del(A)₈	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₁₀	dup(A)₁₄	dup(A)₁₈	ins(A)₂₄	ins(A)₂₅	ins(A)₂₆
GRCh38.p14 chr 11	NC_000011.10:g.74217542_74217563=	NC_000011.10:g.74217550_74217563del	NC_000011.10:g.74217551_74217563del	NC_000011.10:g.74217552_74217563del	NC_000011.10:g.74217553_74217563del	NC_000011.10:g.74217554_74217563del	NC_000011.10:g.74217555_74217563del	NC_000011.10:g.74217556_74217563del	NC_000011.10:g.74217557_74217563del	NC_000011.10:g.74217558_74217563del	NC_000011.10:g.74217559_74217563del	NC_000011.10:g.74217560_74217563del	NC_000011.10:g.74217561_74217563del	NC_000011.10:g.74217562_74217563del	NC_000011.10:g.74217563del	NC_000011.10:g.74217563dup	NC_000011.10:g.74217562_74217563dup	NC_000011.10:g.74217561_74217563dup	NC_000011.10:g.74217560_74217563dup	NC_000011.10:g.74217559_74217563dup	NC_000011.10:g.74217558_74217563dup	NC_000011.10:g.74217557_74217563dup	NC_000011.10:g.74217556_74217563dup	NC_000011.10:g.74217554_74217563dup	NC_000011.10:g.74217550_74217563dup	NC_000011.10:g.74217546_74217563dup	NC_000011.10:g.74217563_74217564insAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:g.74217563_74217564insAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:g.74217563_74217564insAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 11	NC_000011.9:g.73928587_73928608=	NC_000011.9:g.73928595_73928608del	NC_000011.9:g.73928596_73928608del	NC_000011.9:g.73928597_73928608del	NC_000011.9:g.73928598_73928608del	NC_000011.9:g.73928599_73928608del	NC_000011.9:g.73928600_73928608del	NC_000011.9:g.73928601_73928608del	NC_000011.9:g.73928602_73928608del	NC_000011.9:g.73928603_73928608del	NC_000011.9:g.73928604_73928608del	NC_000011.9:g.73928605_73928608del	NC_000011.9:g.73928606_73928608del	NC_000011.9:g.73928607_73928608del	NC_000011.9:g.73928608del	NC_000011.9:g.73928608dup	NC_000011.9:g.73928607_73928608dup	NC_000011.9:g.73928606_73928608dup	NC_000011.9:g.73928605_73928608dup	NC_000011.9:g.73928604_73928608dup	NC_000011.9:g.73928603_73928608dup	NC_000011.9:g.73928602_73928608dup	NC_000011.9:g.73928601_73928608dup	NC_000011.9:g.73928599_73928608dup	NC_000011.9:g.73928595_73928608dup	NC_000011.9:g.73928591_73928608dup	NC_000011.9:g.73928608_73928609insAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.9:g.73928608_73928609insAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.9:g.73928608_73928609insAAAAAAAAAAAAAAAAAAAAAAAAAA
PPME1 transcript variant 2	NM_001271593.1:c.289-4770=	NM_001271593.1:c.289-4762_289-4749del	NM_001271593.1:c.289-4761_289-4749del	NM_001271593.1:c.289-4760_289-4749del	NM_001271593.1:c.289-4759_289-4749del	NM_001271593.1:c.289-4758_289-4749del	NM_001271593.1:c.289-4757_289-4749del	NM_001271593.1:c.289-4756_289-4749del	NM_001271593.1:c.289-4755_289-4749del	NM_001271593.1:c.289-4754_289-4749del	NM_001271593.1:c.289-4753_289-4749del	NM_001271593.1:c.289-4752_289-4749del	NM_001271593.1:c.289-4751_289-4749del	NM_001271593.1:c.289-4750_289-4749del	NM_001271593.1:c.289-4749del	NM_001271593.1:c.289-4749dup	NM_001271593.1:c.289-4750_289-4749dup	NM_001271593.1:c.289-4751_289-4749dup	NM_001271593.1:c.289-4752_289-4749dup	NM_001271593.1:c.289-4753_289-4749dup	NM_001271593.1:c.289-4754_289-4749dup	NM_001271593.1:c.289-4755_289-4749dup	NM_001271593.1:c.289-4756_289-4749dup	NM_001271593.1:c.289-4758_289-4749dup	NM_001271593.1:c.289-4762_289-4749dup	NM_001271593.1:c.289-4766_289-4749dup	NM_001271593.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAA	NM_001271593.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001271593.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAAA
PPME1 transcript variant 2	NM_001271593.2:c.289-4770=	NM_001271593.2:c.289-4762_289-4749del	NM_001271593.2:c.289-4761_289-4749del	NM_001271593.2:c.289-4760_289-4749del	NM_001271593.2:c.289-4759_289-4749del	NM_001271593.2:c.289-4758_289-4749del	NM_001271593.2:c.289-4757_289-4749del	NM_001271593.2:c.289-4756_289-4749del	NM_001271593.2:c.289-4755_289-4749del	NM_001271593.2:c.289-4754_289-4749del	NM_001271593.2:c.289-4753_289-4749del	NM_001271593.2:c.289-4752_289-4749del	NM_001271593.2:c.289-4751_289-4749del	NM_001271593.2:c.289-4750_289-4749del	NM_001271593.2:c.289-4749del	NM_001271593.2:c.289-4749dup	NM_001271593.2:c.289-4750_289-4749dup	NM_001271593.2:c.289-4751_289-4749dup	NM_001271593.2:c.289-4752_289-4749dup	NM_001271593.2:c.289-4753_289-4749dup	NM_001271593.2:c.289-4754_289-4749dup	NM_001271593.2:c.289-4755_289-4749dup	NM_001271593.2:c.289-4756_289-4749dup	NM_001271593.2:c.289-4758_289-4749dup	NM_001271593.2:c.289-4762_289-4749dup	NM_001271593.2:c.289-4766_289-4749dup	NM_001271593.2:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAA	NM_001271593.2:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001271593.2:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAAA
PPME1 transcript variant 1	NM_016147.2:c.289-4770=	NM_016147.2:c.289-4762_289-4749del	NM_016147.2:c.289-4761_289-4749del	NM_016147.2:c.289-4760_289-4749del	NM_016147.2:c.289-4759_289-4749del	NM_016147.2:c.289-4758_289-4749del	NM_016147.2:c.289-4757_289-4749del	NM_016147.2:c.289-4756_289-4749del	NM_016147.2:c.289-4755_289-4749del	NM_016147.2:c.289-4754_289-4749del	NM_016147.2:c.289-4753_289-4749del	NM_016147.2:c.289-4752_289-4749del	NM_016147.2:c.289-4751_289-4749del	NM_016147.2:c.289-4750_289-4749del	NM_016147.2:c.289-4749del	NM_016147.2:c.289-4749dup	NM_016147.2:c.289-4750_289-4749dup	NM_016147.2:c.289-4751_289-4749dup	NM_016147.2:c.289-4752_289-4749dup	NM_016147.2:c.289-4753_289-4749dup	NM_016147.2:c.289-4754_289-4749dup	NM_016147.2:c.289-4755_289-4749dup	NM_016147.2:c.289-4756_289-4749dup	NM_016147.2:c.289-4758_289-4749dup	NM_016147.2:c.289-4762_289-4749dup	NM_016147.2:c.289-4766_289-4749dup	NM_016147.2:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAA	NM_016147.2:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_016147.2:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAAA
PPME1 transcript variant 1	NM_016147.3:c.289-4770=	NM_016147.3:c.289-4762_289-4749del	NM_016147.3:c.289-4761_289-4749del	NM_016147.3:c.289-4760_289-4749del	NM_016147.3:c.289-4759_289-4749del	NM_016147.3:c.289-4758_289-4749del	NM_016147.3:c.289-4757_289-4749del	NM_016147.3:c.289-4756_289-4749del	NM_016147.3:c.289-4755_289-4749del	NM_016147.3:c.289-4754_289-4749del	NM_016147.3:c.289-4753_289-4749del	NM_016147.3:c.289-4752_289-4749del	NM_016147.3:c.289-4751_289-4749del	NM_016147.3:c.289-4750_289-4749del	NM_016147.3:c.289-4749del	NM_016147.3:c.289-4749dup	NM_016147.3:c.289-4750_289-4749dup	NM_016147.3:c.289-4751_289-4749dup	NM_016147.3:c.289-4752_289-4749dup	NM_016147.3:c.289-4753_289-4749dup	NM_016147.3:c.289-4754_289-4749dup	NM_016147.3:c.289-4755_289-4749dup	NM_016147.3:c.289-4756_289-4749dup	NM_016147.3:c.289-4758_289-4749dup	NM_016147.3:c.289-4762_289-4749dup	NM_016147.3:c.289-4766_289-4749dup	NM_016147.3:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAA	NM_016147.3:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_016147.3:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAAA
PPME1 transcript variant X1	XM_005274045.1:c.289-4770=	XM_005274045.1:c.289-4762_289-4749del	XM_005274045.1:c.289-4761_289-4749del	XM_005274045.1:c.289-4760_289-4749del	XM_005274045.1:c.289-4759_289-4749del	XM_005274045.1:c.289-4758_289-4749del	XM_005274045.1:c.289-4757_289-4749del	XM_005274045.1:c.289-4756_289-4749del	XM_005274045.1:c.289-4755_289-4749del	XM_005274045.1:c.289-4754_289-4749del	XM_005274045.1:c.289-4753_289-4749del	XM_005274045.1:c.289-4752_289-4749del	XM_005274045.1:c.289-4751_289-4749del	XM_005274045.1:c.289-4750_289-4749del	XM_005274045.1:c.289-4749del	XM_005274045.1:c.289-4749dup	XM_005274045.1:c.289-4750_289-4749dup	XM_005274045.1:c.289-4751_289-4749dup	XM_005274045.1:c.289-4752_289-4749dup	XM_005274045.1:c.289-4753_289-4749dup	XM_005274045.1:c.289-4754_289-4749dup	XM_005274045.1:c.289-4755_289-4749dup	XM_005274045.1:c.289-4756_289-4749dup	XM_005274045.1:c.289-4758_289-4749dup	XM_005274045.1:c.289-4762_289-4749dup	XM_005274045.1:c.289-4766_289-4749dup	XM_005274045.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAA	XM_005274045.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_005274045.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAAA
PPME1 transcript variant X2	XM_017017913.3:c.289-4770=	XM_017017913.3:c.289-4762_289-4749del	XM_017017913.3:c.289-4761_289-4749del	XM_017017913.3:c.289-4760_289-4749del	XM_017017913.3:c.289-4759_289-4749del	XM_017017913.3:c.289-4758_289-4749del	XM_017017913.3:c.289-4757_289-4749del	XM_017017913.3:c.289-4756_289-4749del	XM_017017913.3:c.289-4755_289-4749del	XM_017017913.3:c.289-4754_289-4749del	XM_017017913.3:c.289-4753_289-4749del	XM_017017913.3:c.289-4752_289-4749del	XM_017017913.3:c.289-4751_289-4749del	XM_017017913.3:c.289-4750_289-4749del	XM_017017913.3:c.289-4749del	XM_017017913.3:c.289-4749dup	XM_017017913.3:c.289-4750_289-4749dup	XM_017017913.3:c.289-4751_289-4749dup	XM_017017913.3:c.289-4752_289-4749dup	XM_017017913.3:c.289-4753_289-4749dup	XM_017017913.3:c.289-4754_289-4749dup	XM_017017913.3:c.289-4755_289-4749dup	XM_017017913.3:c.289-4756_289-4749dup	XM_017017913.3:c.289-4758_289-4749dup	XM_017017913.3:c.289-4762_289-4749dup	XM_017017913.3:c.289-4766_289-4749dup	XM_017017913.3:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAA	XM_017017913.3:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_017017913.3:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAAA
PPME1 transcript variant X1	XM_047427116.1:c.289-4770=	XM_047427116.1:c.289-4762_289-4749del	XM_047427116.1:c.289-4761_289-4749del	XM_047427116.1:c.289-4760_289-4749del	XM_047427116.1:c.289-4759_289-4749del	XM_047427116.1:c.289-4758_289-4749del	XM_047427116.1:c.289-4757_289-4749del	XM_047427116.1:c.289-4756_289-4749del	XM_047427116.1:c.289-4755_289-4749del	XM_047427116.1:c.289-4754_289-4749del	XM_047427116.1:c.289-4753_289-4749del	XM_047427116.1:c.289-4752_289-4749del	XM_047427116.1:c.289-4751_289-4749del	XM_047427116.1:c.289-4750_289-4749del	XM_047427116.1:c.289-4749del	XM_047427116.1:c.289-4749dup	XM_047427116.1:c.289-4750_289-4749dup	XM_047427116.1:c.289-4751_289-4749dup	XM_047427116.1:c.289-4752_289-4749dup	XM_047427116.1:c.289-4753_289-4749dup	XM_047427116.1:c.289-4754_289-4749dup	XM_047427116.1:c.289-4755_289-4749dup	XM_047427116.1:c.289-4756_289-4749dup	XM_047427116.1:c.289-4758_289-4749dup	XM_047427116.1:c.289-4762_289-4749dup	XM_047427116.1:c.289-4766_289-4749dup	XM_047427116.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAA	XM_047427116.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAA	XM_047427116.1:c.289-4749_289-4748insAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

62 SubSNP, 39 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss83268930	Aug 21, 2014 (142)
2	HUMANGENOME_JCVI	ss95572899	Feb 04, 2009 (136)
3	PJP	ss294709841	May 09, 2011 (134)
4	PJP	ss294709842	May 09, 2011 (136)
5	EVA_GENOME_DK	ss1574376544	Apr 01, 2015 (144)
6	EVA_UK10K_ALSPAC	ss1707157863	Apr 01, 2015 (144)
7	EVA_UK10K_TWINSUK	ss1707157990	Apr 01, 2015 (144)
8	EVA_UK10K_TWINSUK	ss1710521039	Apr 01, 2015 (144)
9	EVA_UK10K_ALSPAC	ss1710521048	Apr 01, 2015 (144)
10	SWEGEN	ss3008347428	Nov 08, 2017 (151)
11	EVA_DECODE	ss3692083884	Jul 13, 2019 (153)
12	EVA_DECODE	ss3692083885	Jul 13, 2019 (153)
13	EVA_DECODE	ss3692083886	Jul 13, 2019 (153)
14	EVA_DECODE	ss3692083887	Jul 13, 2019 (153)
15	EVA_DECODE	ss3692083888	Jul 13, 2019 (153)
16	PACBIO	ss3786991989	Jul 13, 2019 (153)
17	PACBIO	ss3792126709	Jul 13, 2019 (153)
18	PACBIO	ss3797009060	Jul 13, 2019 (153)
19	EVA	ss3832700948	Apr 26, 2020 (154)
20	GNOMAD	ss4237830531	Apr 26, 2021 (155)
21	GNOMAD	ss4237830532	Apr 26, 2021 (155)
22	GNOMAD	ss4237830533	Apr 26, 2021 (155)
23	GNOMAD	ss4237830534	Apr 26, 2021 (155)
24	GNOMAD	ss4237830535	Apr 26, 2021 (155)
25	GNOMAD	ss4237830536	Apr 26, 2021 (155)
26	GNOMAD	ss4237830537	Apr 26, 2021 (155)
27	GNOMAD	ss4237830538	Apr 26, 2021 (155)
28	GNOMAD	ss4237830539	Apr 26, 2021 (155)
29	GNOMAD	ss4237830540	Apr 26, 2021 (155)
30	GNOMAD	ss4237830541	Apr 26, 2021 (155)
31	GNOMAD	ss4237830542	Apr 26, 2021 (155)
32	GNOMAD	ss4237830543	Apr 26, 2021 (155)
33	GNOMAD	ss4237830544	Apr 26, 2021 (155)
34	GNOMAD	ss4237830549	Apr 26, 2021 (155)
35	GNOMAD	ss4237830550	Apr 26, 2021 (155)
36	GNOMAD	ss4237830551	Apr 26, 2021 (155)
37	GNOMAD	ss4237830552	Apr 26, 2021 (155)
38	GNOMAD	ss4237830553	Apr 26, 2021 (155)
39	GNOMAD	ss4237830554	Apr 26, 2021 (155)
40	GNOMAD	ss4237830555	Apr 26, 2021 (155)
41	GNOMAD	ss4237830556	Apr 26, 2021 (155)
42	GNOMAD	ss4237830557	Apr 26, 2021 (155)
43	GNOMAD	ss4237830558	Apr 26, 2021 (155)
44	TOMMO_GENOMICS	ss5202693619	Apr 26, 2021 (155)
45	TOMMO_GENOMICS	ss5202693620	Apr 26, 2021 (155)
46	TOMMO_GENOMICS	ss5202693621	Apr 26, 2021 (155)
47	TOMMO_GENOMICS	ss5202693622	Apr 26, 2021 (155)
48	TOMMO_GENOMICS	ss5202693623	Apr 26, 2021 (155)
49	1000G_HIGH_COVERAGE	ss5287964726	Oct 16, 2022 (156)
50	1000G_HIGH_COVERAGE	ss5287964727	Oct 16, 2022 (156)
51	1000G_HIGH_COVERAGE	ss5287964729	Oct 16, 2022 (156)
52	1000G_HIGH_COVERAGE	ss5287964730	Oct 16, 2022 (156)
53	1000G_HIGH_COVERAGE	ss5287964731	Oct 16, 2022 (156)
54	HUGCELL_USP	ss5483067388	Oct 16, 2022 (156)
55	HUGCELL_USP	ss5483067389	Oct 16, 2022 (156)
56	HUGCELL_USP	ss5483067390	Oct 16, 2022 (156)
57	HUGCELL_USP	ss5483067391	Oct 16, 2022 (156)
58	TOMMO_GENOMICS	ss5750802879	Oct 16, 2022 (156)
59	TOMMO_GENOMICS	ss5750802880	Oct 16, 2022 (156)
60	TOMMO_GENOMICS	ss5750802881	Oct 16, 2022 (156)
61	TOMMO_GENOMICS	ss5750802883	Oct 16, 2022 (156)
62	YY_MCH	ss5812547787	Oct 16, 2022 (156)
63	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30211206 (NC_000011.9:73928587:A: 2631/3854) Row 30211207 (NC_000011.9:73928586:AAA: 591/3854)	-	Oct 12, 2018 (152)
64	The Avon Longitudinal Study of Parents and Children Submission ignored due to conflicting rows: Row 30211206 (NC_000011.9:73928587:A: 2631/3854) Row 30211207 (NC_000011.9:73928586:AAA: 591/3854)	-	Oct 12, 2018 (152)
65	The Danish reference pan genome	NC_000011.9 - 73928587	Apr 26, 2020 (154)
66	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
67	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
68	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
69	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
70	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
71	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
72	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
73	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
74	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 384201231 (NC_000011.10:74217541::A 544/72132) Row 384201232 (NC_000011.10:74217541::AA 104/72364) Row 384201233 (NC_000011.10:74217541::AAA 10/72476)...	-	Apr 26, 2021 (155)
90	8.3KJPN Submission ignored due to conflicting rows: Row 60662926 (NC_000011.9:73928586:A: 9147/16560) Row 60662927 (NC_000011.9:73928586:AA: 116/16560) Row 60662928 (NC_000011.9:73928586::A 205/16560)...	-	Apr 26, 2021 (155)
91	8.3KJPN Submission ignored due to conflicting rows: Row 60662926 (NC_000011.9:73928586:A: 9147/16560) Row 60662927 (NC_000011.9:73928586:AA: 116/16560) Row 60662928 (NC_000011.9:73928586::A 205/16560)...	-	Apr 26, 2021 (155)
92	8.3KJPN Submission ignored due to conflicting rows: Row 60662926 (NC_000011.9:73928586:A: 9147/16560) Row 60662927 (NC_000011.9:73928586:AA: 116/16560) Row 60662928 (NC_000011.9:73928586::A 205/16560)...	-	Apr 26, 2021 (155)
93	8.3KJPN Submission ignored due to conflicting rows: Row 60662926 (NC_000011.9:73928586:A: 9147/16560) Row 60662927 (NC_000011.9:73928586:AA: 116/16560) Row 60662928 (NC_000011.9:73928586::A 205/16560)...	-	Apr 26, 2021 (155)
94	8.3KJPN Submission ignored due to conflicting rows: Row 60662926 (NC_000011.9:73928586:A: 9147/16560) Row 60662927 (NC_000011.9:73928586:AA: 116/16560) Row 60662928 (NC_000011.9:73928586::A 205/16560)...	-	Apr 26, 2021 (155)
95	14KJPN Submission ignored due to conflicting rows: Row 84639983 (NC_000011.10:74217541:AA: 213/27468) Row 84639984 (NC_000011.10:74217541:A: 16097/27468) Row 84639985 (NC_000011.10:74217541::A 336/27468)...	-	Oct 16, 2022 (156)
96	14KJPN Submission ignored due to conflicting rows: Row 84639983 (NC_000011.10:74217541:AA: 213/27468) Row 84639984 (NC_000011.10:74217541:A: 16097/27468) Row 84639985 (NC_000011.10:74217541::A 336/27468)...	-	Oct 16, 2022 (156)
97	14KJPN Submission ignored due to conflicting rows: Row 84639983 (NC_000011.10:74217541:AA: 213/27468) Row 84639984 (NC_000011.10:74217541:A: 16097/27468) Row 84639985 (NC_000011.10:74217541::A 336/27468)...	-	Oct 16, 2022 (156)
98	14KJPN Submission ignored due to conflicting rows: Row 84639983 (NC_000011.10:74217541:AA: 213/27468) Row 84639984 (NC_000011.10:74217541:A: 16097/27468) Row 84639985 (NC_000011.10:74217541::A 336/27468)...	-	Oct 16, 2022 (156)
99	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30211206 (NC_000011.9:73928587:A: 2532/3708) Row 30211207 (NC_000011.9:73928586:AAA: 564/3708)	-	Oct 12, 2018 (152)
100	UK 10K study - Twins Submission ignored due to conflicting rows: Row 30211206 (NC_000011.9:73928587:A: 2532/3708) Row 30211207 (NC_000011.9:73928586:AAA: 564/3708)	-	Oct 12, 2018 (152)
101	ALFA	NC_000011.10 - 74217542	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)
rs66614764	Oct 15, 2011 (136)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA	(self)
ss4237830558	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA	(self)
ss4237830557, ss5287964731	NC_000011.10:74217541:AAAAAAAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
ss4237830556	NC_000011.10:74217541:AAAAAAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA	(self)
ss4237830555	NC_000011.10:74217541:AAAAAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA	(self)
ss5202693623	NC_000011.9:73928586:AAAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4237830554, ss5750802883	NC_000011.10:74217541:AAAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
ss4237830553	NC_000011.10:74217541:AAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
ss5202693622	NC_000011.9:73928586:AAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss4237830552	NC_000011.10:74217541:AAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss3692083888, ss4237830551	NC_000011.10:74217541:AAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss1707157863, ss1707157990	NC_000011.9:73928586:AAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4237830550	NC_000011.10:74217541:AAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3692083887	NC_000011.10:74217542:AAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss83268930	NC_000011.8:73606254:AA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3008347428, ss5202693620	NC_000011.9:73928586:AA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss1710521039, ss1710521048	NC_000011.9:73928587:AA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4237830549, ss5287964727, ss5483067389, ss5750802879	NC_000011.10:74217541:AA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3692083886	NC_000011.10:74217543:AA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss294709841	NC_000011.8:73606234:A:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss294709842	NC_000011.8:73606255:A:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
304858, ss1574376544, ss3786991989, ss3792126709, ss3797009060, ss3832700948, ss5202693619	NC_000011.9:73928586:A:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
	NC_000011.9:73928587:A:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5287964726, ss5483067388, ss5750802880, ss5812547787	NC_000011.10:74217541:A:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss3692083885	NC_000011.10:74217544:A:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss95572899	NT_167190.1:19234402:A:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA	(self)
ss5202693621	NC_000011.9:73928586::A	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830531, ss5287964729, ss5483067390, ss5750802881	NC_000011.10:74217541::A	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3692083884	NC_000011.10:74217545::A	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830532, ss5287964730, ss5483067391	NC_000011.10:74217541::AA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830533	NC_000011.10:74217541::AAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830534	NC_000011.10:74217541::AAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830535	NC_000011.10:74217541::AAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830536	NC_000011.10:74217541::AAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830537	NC_000011.10:74217541::AAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
3584191294	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830538	NC_000011.10:74217541::AAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830539	NC_000011.10:74217541::AAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830540	NC_000011.10:74217541::AAAAAAAAAAA… NC_000011.10:74217541::AAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830541	NC_000011.10:74217541::AAAAAAAAAAA… NC_000011.10:74217541::AAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830542	NC_000011.10:74217541::AAAAAAAAAAA… NC_000011.10:74217541::AAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830543	NC_000011.10:74217541::AAAAAAAAAAA… NC_000011.10:74217541::AAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4237830544	NC_000011.10:74217541::AAAAAAAAAAA… NC_000011.10:74217541::AAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3149400204	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAA:	NC_000011.10:74217541:AAAAAAAAAAAA… NC_000011.10:74217541:AAAAAAAAAAAAAAAAAAAAAA:AAAAAAAA

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

No publications for rs61139169

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

rs61139169