Name: rs61549690
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.

rs61549690

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr9:85955361-85955377 (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)₆ / del(T)₅ / del(T)₄ / delT…
del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₄
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₆=0.00000 (0/11660, ALFA)
del(T)₅=0.00000 (0/11660, ALFA)
del(T)₄=0.00000 (0/11660, ALFA) (+ 16 more)
delTTT=0.00000 (0/11660, ALFA)
delTT=0.00000 (0/11660, ALFA)
delT=0.00000 (0/11660, ALFA)
dupT=0.00000 (0/11660, ALFA)
dupTT=0.00000 (0/11660, ALFA)
dupTTT=0.00000 (0/11660, ALFA)
dup(T)₄=0.00000 (0/11660, ALFA)
dup(T)₅=0.00000 (0/11660, ALFA)
dup(T)₆=0.00000 (0/11660, ALFA)
dup(T)₇=0.00000 (0/11660, ALFA)
dup(T)₈=0.00000 (0/11660, ALFA)
dup(T)₉=0.00000 (0/11660, ALFA)
dup(T)₁₁=0.00000 (0/11660, ALFA)
dup(T)₁₂=0.00000 (0/11660, ALFA)
dup(T)₁₃=0.00000 (0/11660, ALFA)
dup(T)₄=0.25 (10/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: NAA35 : 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	11660	TTTTTTTTTTTTTTTTT=1.00000	TTTTTTTTTTT=0.00000, TTTTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00000	1.0	N/A
European	Sub	7534	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African	Sub	2748	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
African Others	Sub	106	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
African American	Sub	2642	TTTTTTTTTTTTTTTTT=1.0000	TTTTTTTTTTT=0.0000, TTTTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0000	1.0	N/A
Asian	Sub	102	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
East Asian	Sub	80	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other Asian	Sub	22	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Latin American 1	Sub	146	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
Latin American 2	Sub	592	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	N/A
South Asian	Sub	84	TTTTTTTTTTTTTTTTT=1.00	TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	N/A
Other	Sub	454	TTTTTTTTTTTTTTTTT=1.000	TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT=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	11660	(T)₁₇=1.00000	del(T)₆=0.00000, del(T)₅=0.00000, del(T)₄=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00000, dupT=0.00000, dupTT=0.00000, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₅=0.00000, dup(T)₆=0.00000, dup(T)₇=0.00000, dup(T)₈=0.00000, dup(T)₉=0.00000, dup(T)₁₁=0.00000, dup(T)₁₂=0.00000, dup(T)₁₃=0.00000
Allele Frequency Aggregator	European	Sub	7534	(T)₁₇=1.0000	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, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₁=0.0000, dup(T)₁₂=0.0000, dup(T)₁₃=0.0000
Allele Frequency Aggregator	African	Sub	2748	(T)₁₇=1.0000	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, dup(T)₆=0.0000, dup(T)₇=0.0000, dup(T)₈=0.0000, dup(T)₉=0.0000, dup(T)₁₁=0.0000, dup(T)₁₂=0.0000, dup(T)₁₃=0.0000
Allele Frequency Aggregator	Latin American 2	Sub	592	(T)₁₇=1.000	del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₃=0.000
Allele Frequency Aggregator	Other	Sub	454	(T)₁₇=1.000	del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	146	(T)₁₇=1.000	del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₃=0.000
Allele Frequency Aggregator	Asian	Sub	102	(T)₁₇=1.000	del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000, dup(T)₈=0.000, dup(T)₉=0.000, dup(T)₁₁=0.000, dup(T)₁₂=0.000, dup(T)₁₃=0.000
Allele Frequency Aggregator	South Asian	Sub	84	(T)₁₇=1.00	del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00, dup(T)₈=0.00, dup(T)₉=0.00, dup(T)₁₁=0.00, dup(T)₁₂=0.00, dup(T)₁₃=0.00
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dup(T)₄=0.25

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 9	NC_000009.12:g.85955372_85955377del
GRCh38.p14 chr 9	NC_000009.12:g.85955373_85955377del
GRCh38.p14 chr 9	NC_000009.12:g.85955374_85955377del
GRCh38.p14 chr 9	NC_000009.12:g.85955375_85955377del
GRCh38.p14 chr 9	NC_000009.12:g.85955376_85955377del
GRCh38.p14 chr 9	NC_000009.12:g.85955377del
GRCh38.p14 chr 9	NC_000009.12:g.85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955376_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955375_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955374_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955373_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955372_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955371_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955370_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955369_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955368_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955367_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955366_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955365_85955377dup
GRCh38.p14 chr 9	NC_000009.12:g.85955364_85955377dup
GRCh37.p13 chr 9	NC_000009.11:g.88570287_88570292del
GRCh37.p13 chr 9	NC_000009.11:g.88570288_88570292del
GRCh37.p13 chr 9	NC_000009.11:g.88570289_88570292del
GRCh37.p13 chr 9	NC_000009.11:g.88570290_88570292del
GRCh37.p13 chr 9	NC_000009.11:g.88570291_88570292del
GRCh37.p13 chr 9	NC_000009.11:g.88570292del
GRCh37.p13 chr 9	NC_000009.11:g.88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570291_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570290_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570289_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570288_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570287_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570286_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570285_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570284_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570283_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570282_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570281_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570280_88570292dup
GRCh37.p13 chr 9	NC_000009.11:g.88570279_88570292dup

Gene: NAA35, N-alpha-acetyltransferase 35, NatC auxiliary subunit (plus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
NAA35 transcript variant 2	NM_001321881.2:c.125-988_… NM_001321881.2:c.125-988_125-983del	N/A	Intron Variant
NAA35 transcript variant 3	NM_001321882.2:c.125-988_… NM_001321882.2:c.125-988_125-983del	N/A	Intron Variant
NAA35 transcript variant 1	NM_024635.4:c.125-988_125… NM_024635.4:c.125-988_125-983del	N/A	Intron Variant
NAA35 transcript variant X1	XM_005252127.5:c.125-988_… XM_005252127.5:c.125-988_125-983del	N/A	Intron Variant
NAA35 transcript variant X3	XM_024447648.2:c.	N/A	Genic Upstream Transcript Variant
NAA35 transcript variant X4	XM_024447649.2:c.	N/A	Genic Upstream Transcript Variant
NAA35 transcript variant X2	XM_047423710.1:c.	N/A	Genic Upstream Transcript Variant

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

Not Reported in ClinVar

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

Placement	(T)₁₇=	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₄
GRCh38.p14 chr 9	NC_000009.12:g.85955361_85955377=	NC_000009.12:g.85955372_85955377del	NC_000009.12:g.85955373_85955377del	NC_000009.12:g.85955374_85955377del	NC_000009.12:g.85955375_85955377del	NC_000009.12:g.85955376_85955377del	NC_000009.12:g.85955377del	NC_000009.12:g.85955377dup	NC_000009.12:g.85955376_85955377dup	NC_000009.12:g.85955375_85955377dup	NC_000009.12:g.85955374_85955377dup	NC_000009.12:g.85955373_85955377dup	NC_000009.12:g.85955372_85955377dup	NC_000009.12:g.85955371_85955377dup	NC_000009.12:g.85955370_85955377dup	NC_000009.12:g.85955369_85955377dup	NC_000009.12:g.85955368_85955377dup	NC_000009.12:g.85955367_85955377dup	NC_000009.12:g.85955366_85955377dup	NC_000009.12:g.85955365_85955377dup	NC_000009.12:g.85955364_85955377dup
GRCh37.p13 chr 9	NC_000009.11:g.88570276_88570292=	NC_000009.11:g.88570287_88570292del	NC_000009.11:g.88570288_88570292del	NC_000009.11:g.88570289_88570292del	NC_000009.11:g.88570290_88570292del	NC_000009.11:g.88570291_88570292del	NC_000009.11:g.88570292del	NC_000009.11:g.88570292dup	NC_000009.11:g.88570291_88570292dup	NC_000009.11:g.88570290_88570292dup	NC_000009.11:g.88570289_88570292dup	NC_000009.11:g.88570288_88570292dup	NC_000009.11:g.88570287_88570292dup	NC_000009.11:g.88570286_88570292dup	NC_000009.11:g.88570285_88570292dup	NC_000009.11:g.88570284_88570292dup	NC_000009.11:g.88570283_88570292dup	NC_000009.11:g.88570282_88570292dup	NC_000009.11:g.88570281_88570292dup	NC_000009.11:g.88570280_88570292dup	NC_000009.11:g.88570279_88570292dup
NAA35 transcript variant 2	NM_001321881.2:c.125-999=	NM_001321881.2:c.125-988_125-983del	NM_001321881.2:c.125-987_125-983del	NM_001321881.2:c.125-986_125-983del	NM_001321881.2:c.125-985_125-983del	NM_001321881.2:c.125-984_125-983del	NM_001321881.2:c.125-983del	NM_001321881.2:c.125-983dup	NM_001321881.2:c.125-984_125-983dup	NM_001321881.2:c.125-985_125-983dup	NM_001321881.2:c.125-986_125-983dup	NM_001321881.2:c.125-987_125-983dup	NM_001321881.2:c.125-988_125-983dup	NM_001321881.2:c.125-989_125-983dup	NM_001321881.2:c.125-990_125-983dup	NM_001321881.2:c.125-991_125-983dup	NM_001321881.2:c.125-992_125-983dup	NM_001321881.2:c.125-993_125-983dup	NM_001321881.2:c.125-994_125-983dup	NM_001321881.2:c.125-995_125-983dup	NM_001321881.2:c.125-996_125-983dup
NAA35 transcript variant 3	NM_001321882.2:c.125-999=	NM_001321882.2:c.125-988_125-983del	NM_001321882.2:c.125-987_125-983del	NM_001321882.2:c.125-986_125-983del	NM_001321882.2:c.125-985_125-983del	NM_001321882.2:c.125-984_125-983del	NM_001321882.2:c.125-983del	NM_001321882.2:c.125-983dup	NM_001321882.2:c.125-984_125-983dup	NM_001321882.2:c.125-985_125-983dup	NM_001321882.2:c.125-986_125-983dup	NM_001321882.2:c.125-987_125-983dup	NM_001321882.2:c.125-988_125-983dup	NM_001321882.2:c.125-989_125-983dup	NM_001321882.2:c.125-990_125-983dup	NM_001321882.2:c.125-991_125-983dup	NM_001321882.2:c.125-992_125-983dup	NM_001321882.2:c.125-993_125-983dup	NM_001321882.2:c.125-994_125-983dup	NM_001321882.2:c.125-995_125-983dup	NM_001321882.2:c.125-996_125-983dup
NAA35 transcript variant 1	NM_024635.3:c.125-999=	NM_024635.3:c.125-988_125-983del	NM_024635.3:c.125-987_125-983del	NM_024635.3:c.125-986_125-983del	NM_024635.3:c.125-985_125-983del	NM_024635.3:c.125-984_125-983del	NM_024635.3:c.125-983del	NM_024635.3:c.125-983dup	NM_024635.3:c.125-984_125-983dup	NM_024635.3:c.125-985_125-983dup	NM_024635.3:c.125-986_125-983dup	NM_024635.3:c.125-987_125-983dup	NM_024635.3:c.125-988_125-983dup	NM_024635.3:c.125-989_125-983dup	NM_024635.3:c.125-990_125-983dup	NM_024635.3:c.125-991_125-983dup	NM_024635.3:c.125-992_125-983dup	NM_024635.3:c.125-993_125-983dup	NM_024635.3:c.125-994_125-983dup	NM_024635.3:c.125-995_125-983dup	NM_024635.3:c.125-996_125-983dup
NAA35 transcript variant 1	NM_024635.4:c.125-999=	NM_024635.4:c.125-988_125-983del	NM_024635.4:c.125-987_125-983del	NM_024635.4:c.125-986_125-983del	NM_024635.4:c.125-985_125-983del	NM_024635.4:c.125-984_125-983del	NM_024635.4:c.125-983del	NM_024635.4:c.125-983dup	NM_024635.4:c.125-984_125-983dup	NM_024635.4:c.125-985_125-983dup	NM_024635.4:c.125-986_125-983dup	NM_024635.4:c.125-987_125-983dup	NM_024635.4:c.125-988_125-983dup	NM_024635.4:c.125-989_125-983dup	NM_024635.4:c.125-990_125-983dup	NM_024635.4:c.125-991_125-983dup	NM_024635.4:c.125-992_125-983dup	NM_024635.4:c.125-993_125-983dup	NM_024635.4:c.125-994_125-983dup	NM_024635.4:c.125-995_125-983dup	NM_024635.4:c.125-996_125-983dup
NAA35 transcript variant X1	XM_005252125.1:c.248-999=	XM_005252125.1:c.248-988_248-983del	XM_005252125.1:c.248-987_248-983del	XM_005252125.1:c.248-986_248-983del	XM_005252125.1:c.248-985_248-983del	XM_005252125.1:c.248-984_248-983del	XM_005252125.1:c.248-983del	XM_005252125.1:c.248-983dup	XM_005252125.1:c.248-984_248-983dup	XM_005252125.1:c.248-985_248-983dup	XM_005252125.1:c.248-986_248-983dup	XM_005252125.1:c.248-987_248-983dup	XM_005252125.1:c.248-988_248-983dup	XM_005252125.1:c.248-989_248-983dup	XM_005252125.1:c.248-990_248-983dup	XM_005252125.1:c.248-991_248-983dup	XM_005252125.1:c.248-992_248-983dup	XM_005252125.1:c.248-993_248-983dup	XM_005252125.1:c.248-994_248-983dup	XM_005252125.1:c.248-995_248-983dup	XM_005252125.1:c.248-996_248-983dup
NAA35 transcript variant X2	XM_005252126.1:c.125-999=	XM_005252126.1:c.125-988_125-983del	XM_005252126.1:c.125-987_125-983del	XM_005252126.1:c.125-986_125-983del	XM_005252126.1:c.125-985_125-983del	XM_005252126.1:c.125-984_125-983del	XM_005252126.1:c.125-983del	XM_005252126.1:c.125-983dup	XM_005252126.1:c.125-984_125-983dup	XM_005252126.1:c.125-985_125-983dup	XM_005252126.1:c.125-986_125-983dup	XM_005252126.1:c.125-987_125-983dup	XM_005252126.1:c.125-988_125-983dup	XM_005252126.1:c.125-989_125-983dup	XM_005252126.1:c.125-990_125-983dup	XM_005252126.1:c.125-991_125-983dup	XM_005252126.1:c.125-992_125-983dup	XM_005252126.1:c.125-993_125-983dup	XM_005252126.1:c.125-994_125-983dup	XM_005252126.1:c.125-995_125-983dup	XM_005252126.1:c.125-996_125-983dup
NAA35 transcript variant X3	XM_005252127.1:c.125-999=	XM_005252127.1:c.125-988_125-983del	XM_005252127.1:c.125-987_125-983del	XM_005252127.1:c.125-986_125-983del	XM_005252127.1:c.125-985_125-983del	XM_005252127.1:c.125-984_125-983del	XM_005252127.1:c.125-983del	XM_005252127.1:c.125-983dup	XM_005252127.1:c.125-984_125-983dup	XM_005252127.1:c.125-985_125-983dup	XM_005252127.1:c.125-986_125-983dup	XM_005252127.1:c.125-987_125-983dup	XM_005252127.1:c.125-988_125-983dup	XM_005252127.1:c.125-989_125-983dup	XM_005252127.1:c.125-990_125-983dup	XM_005252127.1:c.125-991_125-983dup	XM_005252127.1:c.125-992_125-983dup	XM_005252127.1:c.125-993_125-983dup	XM_005252127.1:c.125-994_125-983dup	XM_005252127.1:c.125-995_125-983dup	XM_005252127.1:c.125-996_125-983dup
NAA35 transcript variant X1	XM_005252127.5:c.125-999=	XM_005252127.5:c.125-988_125-983del	XM_005252127.5:c.125-987_125-983del	XM_005252127.5:c.125-986_125-983del	XM_005252127.5:c.125-985_125-983del	XM_005252127.5:c.125-984_125-983del	XM_005252127.5:c.125-983del	XM_005252127.5:c.125-983dup	XM_005252127.5:c.125-984_125-983dup	XM_005252127.5:c.125-985_125-983dup	XM_005252127.5:c.125-986_125-983dup	XM_005252127.5:c.125-987_125-983dup	XM_005252127.5:c.125-988_125-983dup	XM_005252127.5:c.125-989_125-983dup	XM_005252127.5:c.125-990_125-983dup	XM_005252127.5:c.125-991_125-983dup	XM_005252127.5:c.125-992_125-983dup	XM_005252127.5:c.125-993_125-983dup	XM_005252127.5:c.125-994_125-983dup	XM_005252127.5:c.125-995_125-983dup	XM_005252127.5:c.125-996_125-983dup

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#.

29 SubSNP, 20 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss81764827	Dec 16, 2007 (129)
2	HGSV	ss81908781	Dec 16, 2007 (129)
3	HUMANGENOME_JCVI	ss95519981	Mar 15, 2016 (147)
4	EVA_GENOME_DK	ss1577412044	Apr 01, 2015 (144)
5	EVA_DECODE	ss3724225425	Jul 13, 2019 (153)
6	EVA_DECODE	ss3724225426	Jul 13, 2019 (153)
7	EVA_DECODE	ss3724225427	Jul 13, 2019 (153)
8	EVA_DECODE	ss3724225428	Jul 13, 2019 (153)
9	EVA_DECODE	ss3724225429	Jul 13, 2019 (153)
10	EVA_DECODE	ss3724225430	Jul 13, 2019 (153)
11	EVA_DECODE	ss3724225432	Jul 13, 2019 (153)
12	GNOMAD	ss4204829035	Apr 26, 2021 (155)
13	GNOMAD	ss4204829071	Apr 26, 2021 (155)
14	GNOMAD	ss4204829072	Apr 26, 2021 (155)
15	GNOMAD	ss4204829073	Apr 26, 2021 (155)
16	GNOMAD	ss4204829074	Apr 26, 2021 (155)
17	GNOMAD	ss4204829075	Apr 26, 2021 (155)
18	GNOMAD	ss4204829076	Apr 26, 2021 (155)
19	GNOMAD	ss4204829077	Apr 26, 2021 (155)
20	GNOMAD	ss4204829078	Apr 26, 2021 (155)
21	GNOMAD	ss4204829079	Apr 26, 2021 (155)
22	GNOMAD	ss4204829080	Apr 26, 2021 (155)
23	GNOMAD	ss4204829081	Apr 26, 2021 (155)
24	GNOMAD	ss4204829082	Apr 26, 2021 (155)
25	GNOMAD	ss4204829083	Apr 26, 2021 (155)
26	GNOMAD	ss4204829084	Apr 26, 2021 (155)
27	TOMMO_GENOMICS	ss5738254865	Oct 13, 2022 (156)
28	TOMMO_GENOMICS	ss5738254867	Oct 13, 2022 (156)
29	TOMMO_GENOMICS	ss5738254868	Oct 13, 2022 (156)
30	The Danish reference pan genome	NC_000009.11 - 88570276	Apr 26, 2020 (154)
31	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
32	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
33	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
34	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
35	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
36	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
37	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
38	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
39	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
40	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
41	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
42	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
43	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
44	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 329965279 (NC_000009.12:85955360::T 14/51462) Row 329965315 (NC_000009.12:85955360::TT 294/51420) Row 329965316 (NC_000009.12:85955360::TTT 29/51458)...	-	Apr 26, 2021 (155)
46	14KJPN Submission ignored due to conflicting rows: Row 72091969 (NC_000009.12:85955360::TT 248/23182) Row 72091971 (NC_000009.12:85955360:TT: 170/23182) Row 72091972 (NC_000009.12:85955360:T: 360/23182)	-	Oct 13, 2022 (156)
47	14KJPN Submission ignored due to conflicting rows: Row 72091969 (NC_000009.12:85955360::TT 248/23182) Row 72091971 (NC_000009.12:85955360:TT: 170/23182) Row 72091972 (NC_000009.12:85955360:T: 360/23182)	-	Oct 13, 2022 (156)
48	14KJPN Submission ignored due to conflicting rows: Row 72091969 (NC_000009.12:85955360::TT 248/23182) Row 72091971 (NC_000009.12:85955360:TT: 170/23182) Row 72091972 (NC_000009.12:85955360:T: 360/23182)	-	Oct 13, 2022 (156)
49	ALFA	NC_000009.12 - 85955361	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)
rs72014610	May 11, 2012 (137)
rs72014779	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4204829084	NC_000009.12:85955360:TTT:	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4204829083, ss5738254867	NC_000009.12:85955360:TT:	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4204829082, ss5738254868	NC_000009.12:85955360:T:	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss95519981	NT_008470.19:17734823:T:	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT	(self)
ss4204829035	NC_000009.12:85955360::T	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss95519981	NT_008470.19:17734823:T:TT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss81764827, ss81908781	NT_008470.19:17734824::T	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3724225425, ss4204829071, ss5738254865	NC_000009.12:85955360::TT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3724225426, ss4204829072	NC_000009.12:85955360::TTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
1285969, ss1577412044	NC_000009.11:88570275::TTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3724225427, ss4204829073	NC_000009.12:85955360::TTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3724225432	NC_000009.12:85955377::TTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3724225428, ss4204829074	NC_000009.12:85955360::TTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3724225429, ss4204829075	NC_000009.12:85955360::TTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204829076	NC_000009.12:85955360::TTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204829077	NC_000009.12:85955360::TTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204829078	NC_000009.12:85955360::TTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204829079	NC_000009.12:85955360::TTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss3724225430, ss4204829080	NC_000009.12:85955360::TTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6962692315	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4204829081	NC_000009.12:85955360::TTTTTTTTTTT… NC_000009.12:85955360::TTTTTTTTTTTTTT	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3593666849	NC_000009.12:85955360:TTTT:	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT
ss3593666850	NC_000009.12:85955360:TTTTT:	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT
ss3593666851	NC_000009.12:85955360:TTTTTT:	NC_000009.12:85955360:TTTTTTTTTTTT… NC_000009.12:85955360:TTTTTTTTTTTTTTTTT: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 rs61549690

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

rs61549690