Name: rs573623299
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.

rs573623299

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr3:180670640-180670655 (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)₇ / del(T)₆ / del(T)₄ / delT…
del(T)₇ / del(T)₆ / del(T)₄ / delTTT / delTT / delT / dupT / ins(TCTT)₂TTTTTTTTTTTTTTTTTTTTTTTTTT / ins(TCTTTTTTT)₂TTTTTTTTTTTT / insTC(T)₁₇ / insTC(T)₁₈ / insTC(T)₂₉ / insTG(T)₉C(T)₁₈ / insTG(T)₉C(T)₁₉ / dupTT / ins(TTCT)₂TTTTTTTTTTTTTTTTTTTTTTTTTTT / ins(TTCTTTTTT)₂TTTTTTTTTTT / ins(TTCTTTTTT)₂TTTTTTTTTTTTT / ins(TTCTTTTTT)₂TTTTTTTTTTTTTTTTTTTTT / insTTC(T)₁₇ / insTTC(T)₁₉ / dupTTT / dup(T)₄ / ins(T)₅C(T)₁₈ / ins(T)₆C(T)₁₈ / ins(T)₆C(T)₁₉ / ins(T)₆C(T)₂₈ / dup(T)₉ / dup(T)₁₀ / ins(T)₁₀C(T)₁₇ / ins(T)₁₀C(T)₁₈ / ins(T)₁₀C(T)₁₉ / dup(T)₁₁ / ins(T)₁₁C(T)₁₇ / ins(T)₁₁C(T)₁₈ / ins(T)₁₁C(T)₁₉ / dup(T)₁₂ / ins(T)₁₂C(T)₂₀ / dup(T)₁₃ / ins(T)₁₈C(T)₁₈ / ins(T)₂₀ / ins(T)₂₀C(T)₁₉ / ins(T)₂₅ / ins(T)₃₀ / ins(T)₃₂ / ins(T)₃₇ / ins(T)₃₈ / ins(T)₄₇
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₆=0.000004 (1/264690, TOPMED)
dupT=0.05394 (596/11050, ALFA)
dupT=0.2402 (1203/5008, 1000G) (+ 1 more)
dupT=0.20 (8/40, GENOME_DK)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: CCDC39 : 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	11050	TTTTTTTTTTTTTTTT=0.94398	TTTTTTTTT=0.00000, TTTTTTTTTT=0.00000, TTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTT=0.00045, TTTTTTTTTTTTTTTTT=0.05394, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00045, TTTTTTTTTTTTTTTTTT=0.00118, TTTTTTTTTTTTTTTTTTT=0.00000, TTTTTTTTTTTTTTTTTTTT=0.00000	0.901327	0.008723	0.089951	32
European	Sub	9362	TTTTTTTTTTTTTTTT=0.9341	TTTTTTTTT=0.0000, TTTTTTTTTT=0.0000, TTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTT=0.0634, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.0005, TTTTTTTTTTTTTTTTTT=0.0014, TTTTTTTTTTTTTTTTTTT=0.0000, TTTTTTTTTTTTTTTTTTTT=0.0000	0.883881	0.010303	0.105817	28
African	Sub	944	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	36	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
African American	Sub	908	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	40	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
East Asian	Sub	28	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other Asian	Sub	12	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 1	Sub	66	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Latin American 2	Sub	312	TTTTTTTTTTTTTTTT=1.000	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
South Asian	Sub	58	TTTTTTTTTTTTTTTT=1.00	TTTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A
Other	Sub	268	TTTTTTTTTTTTTTTT=0.993	TTTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.007, TTTTTTTTTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000	0.985075	0.0	0.014925	0

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

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
TopMed	Global	Study-wide	264690	(T)₁₆=0.999996	del(T)₆=0.000004
Allele Frequency Aggregator	Total	Global	11050	(T)₁₆=0.94398	del(T)₇=0.00000, del(T)₆=0.00000, delTTT=0.00000, delTT=0.00000, delT=0.00045, dupT=0.05394, dupTT=0.00118, dupTTT=0.00000, dup(T)₄=0.00000, dup(T)₁₃=0.00045
Allele Frequency Aggregator	European	Sub	9362	(T)₁₆=0.9341	del(T)₇=0.0000, del(T)₆=0.0000, delTTT=0.0000, delTT=0.0000, delT=0.0005, dupT=0.0634, dupTT=0.0014, dupTTT=0.0000, dup(T)₄=0.0000, dup(T)₁₃=0.0005
Allele Frequency Aggregator	African	Sub	944	(T)₁₆=1.000	del(T)₇=0.000, del(T)₆=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)₁₃=0.000
Allele Frequency Aggregator	Latin American 2	Sub	312	(T)₁₆=1.000	del(T)₇=0.000, del(T)₆=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)₁₃=0.000
Allele Frequency Aggregator	Other	Sub	268	(T)₁₆=0.993	del(T)₇=0.000, del(T)₆=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.007, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₁₃=0.000
Allele Frequency Aggregator	Latin American 1	Sub	66	(T)₁₆=1.00	del(T)₇=0.00, del(T)₆=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)₁₃=0.00
Allele Frequency Aggregator	South Asian	Sub	58	(T)₁₆=1.00	del(T)₇=0.00, del(T)₆=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)₁₃=0.00
Allele Frequency Aggregator	Asian	Sub	40	(T)₁₆=1.00	del(T)₇=0.00, del(T)₆=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)₁₃=0.00
1000Genomes	Global	Study-wide	5008	- No frequency provided	dupT=0.2402
1000Genomes	African	Sub	1322	- No frequency provided	dupT=0.2519
1000Genomes	East Asian	Sub	1008	- No frequency provided	dupT=0.2817
1000Genomes	Europe	Sub	1006	- No frequency provided	dupT=0.2137
1000Genomes	South Asian	Sub	978	- No frequency provided	dupT=0.219
1000Genomes	American	Sub	694	- No frequency provided	dupT=0.226
The Danish reference pan genome	Danish	Study-wide	40	- No frequency provided	dupT=0.20

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 3	NC_000003.12:g.180670649_180670655del
GRCh38.p14 chr 3	NC_000003.12:g.180670650_180670655del
GRCh38.p14 chr 3	NC_000003.12:g.180670652_180670655del
GRCh38.p14 chr 3	NC_000003.12:g.180670653_180670655del
GRCh38.p14 chr 3	NC_000003.12:g.180670654_180670655del
GRCh38.p14 chr 3	NC_000003.12:g.180670655del
GRCh38.p14 chr 3	NC_000003.12:g.180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[17]CTTT[2]T[25]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTT[2]T[11]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670654_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[18]CTTT[2]T[25]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTT[2]T[9]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTT[2]T[11]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTT[2]T[19]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670653_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670652_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[21]CTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[22]CTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[22]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[22]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670647_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670646_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[26]CTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[26]CTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[26]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670645_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[27]CTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[27]CTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[27]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670644_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[28]CTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670643_180670655dup
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[34]CTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655T[36]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 3	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 3	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388437_180388443del
GRCh37.p13 chr 3	NC_000003.11:g.180388438_180388443del
GRCh37.p13 chr 3	NC_000003.11:g.180388440_180388443del
GRCh37.p13 chr 3	NC_000003.11:g.180388441_180388443del
GRCh37.p13 chr 3	NC_000003.11:g.180388442_180388443del
GRCh37.p13 chr 3	NC_000003.11:g.180388443del
GRCh37.p13 chr 3	NC_000003.11:g.180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[17]CTTT[2]T[25]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTT[2]T[11]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388442_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[18]CTTT[2]T[25]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTT[2]T[9]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTT[2]T[11]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTT[2]T[19]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388441_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388440_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[21]CTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[22]CTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[22]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[22]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388435_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388434_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[26]CTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[26]CTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[26]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388433_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[27]CTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[27]CTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[27]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388432_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[28]CTTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388431_180388443dup
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[34]CTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443T[36]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 3	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
CCDC39 RefSeqGene	NG_029581.1:g.13850_13856del
CCDC39 RefSeqGene	NG_029581.1:g.13851_13856del
CCDC39 RefSeqGene	NG_029581.1:g.13853_13856del
CCDC39 RefSeqGene	NG_029581.1:g.13854_13856del
CCDC39 RefSeqGene	NG_029581.1:g.13855_13856del
CCDC39 RefSeqGene	NG_029581.1:g.13856del
CCDC39 RefSeqGene	NG_029581.1:g.13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[28]GAAA[2]A[14]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAA[2]A[9]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[29]GAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[18]GAAAAAAAAACAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAAACAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13855_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[28]GAAA[2]A[15]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[17]GAAAAAAAA[2]A[10]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAA[2]A[10]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[27]GAAAAAAAA[2]A[10]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13854_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13853_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[28]GAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13848_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13847_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13846_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13845_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[20]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13844_13856dup
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAA
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
CCDC39 RefSeqGene	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAA
CCDC39 RefSeqGene	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CCDC39 RefSeqGene	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CCDC39 RefSeqGene	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CCDC39 RefSeqGene	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CCDC39 RefSeqGene	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: CCDC39, coiled-coil domain containing 39 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
CCDC39 transcript	NM_181426.2:c.91-6660_91-… NM_181426.2:c.91-6660_91-6654del	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)₁₆=	del(T)₇	del(T)₆	del(T)₄	delTTT	delTT	delT	dupT	ins(TCTT)₂TTTTTTTTTTTTTTTTTTTTTTTTTT	ins(TCTTTTTTT)₂TTTTTTTTTTTT	insTC(T)₁₇	insTC(T)₁₈	insTC(T)₂₉	insTG(T)₉C(T)₁₈	insTG(T)₉C(T)₁₉	dupTT	ins(TTCT)₂TTTTTTTTTTTTTTTTTTTTTTTTTTT	ins(TTCTTTTTT)₂TTTTTTTTTTT	ins(TTCTTTTTT)₂TTTTTTTTTTTTT	ins(TTCTTTTTT)₂TTTTTTTTTTTTTTTTTTTTT	insTTC(T)₁₇	insTTC(T)₁₉	dupTTT	dup(T)₄	ins(T)₅C(T)₁₈	ins(T)₆C(T)₁₈	ins(T)₆C(T)₁₉	ins(T)₆C(T)₂₈	dup(T)₉	dup(T)₁₀	ins(T)₁₀C(T)₁₇	ins(T)₁₀C(T)₁₈	ins(T)₁₀C(T)₁₉	dup(T)₁₁	ins(T)₁₁C(T)₁₇	ins(T)₁₁C(T)₁₈	ins(T)₁₁C(T)₁₉	dup(T)₁₂	ins(T)₁₂C(T)₂₀	dup(T)₁₃	ins(T)₁₈C(T)₁₈	ins(T)₂₀	ins(T)₂₀C(T)₁₉	ins(T)₂₅	ins(T)₃₀	ins(T)₃₂	ins(T)₃₇	ins(T)₃₈	ins(T)₄₇
GRCh38.p14 chr 3	NC_000003.12:g.180670640_180670655=	NC_000003.12:g.180670649_180670655del	NC_000003.12:g.180670650_180670655del	NC_000003.12:g.180670652_180670655del	NC_000003.12:g.180670653_180670655del	NC_000003.12:g.180670654_180670655del	NC_000003.12:g.180670655del	NC_000003.12:g.180670655dup	NC_000003.12:g.180670640_180670655T[17]CTTT[2]T[25]	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTT[2]T[11]	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[17]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670654_180670655dup	NC_000003.12:g.180670640_180670655T[18]CTTT[2]T[25]	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTT[2]T[9]	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTT[2]T[11]	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTT[2]T[19]	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[18]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670653_180670655dup	NC_000003.12:g.180670652_180670655dup	NC_000003.12:g.180670640_180670655T[21]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[22]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[22]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[22]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670647_180670655dup	NC_000003.12:g.180670646_180670655dup	NC_000003.12:g.180670640_180670655T[26]CTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[26]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[26]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670645_180670655dup	NC_000003.12:g.180670640_180670655T[27]CTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[27]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670640_180670655T[27]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670644_180670655dup	NC_000003.12:g.180670640_180670655T[28]CTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670643_180670655dup	NC_000003.12:g.180670640_180670655T[34]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.180670640_180670655T[36]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:g.180670655_180670656insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 3	NC_000003.11:g.180388428_180388443=	NC_000003.11:g.180388437_180388443del	NC_000003.11:g.180388438_180388443del	NC_000003.11:g.180388440_180388443del	NC_000003.11:g.180388441_180388443del	NC_000003.11:g.180388442_180388443del	NC_000003.11:g.180388443del	NC_000003.11:g.180388443dup	NC_000003.11:g.180388428_180388443T[17]CTTT[2]T[25]	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTT[2]T[11]	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[17]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[17]GTTTTTTTTTCTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388442_180388443dup	NC_000003.11:g.180388428_180388443T[18]CTTT[2]T[25]	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTT[2]T[9]	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTT[2]T[11]	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTT[2]T[19]	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[18]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388441_180388443dup	NC_000003.11:g.180388440_180388443dup	NC_000003.11:g.180388428_180388443T[21]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[22]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[22]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[22]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388435_180388443dup	NC_000003.11:g.180388434_180388443dup	NC_000003.11:g.180388428_180388443T[26]CTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[26]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[26]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388433_180388443dup	NC_000003.11:g.180388428_180388443T[27]CTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[27]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388428_180388443T[27]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388432_180388443dup	NC_000003.11:g.180388428_180388443T[28]CTTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388431_180388443dup	NC_000003.11:g.180388428_180388443T[34]CTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.180388428_180388443T[36]CTTTTTTTTTTTTTTTTTTT[1]	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.11:g.180388443_180388444insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
CCDC39 RefSeqGene	NG_029581.1:g.13841_13856=	NG_029581.1:g.13850_13856del	NG_029581.1:g.13851_13856del	NG_029581.1:g.13853_13856del	NG_029581.1:g.13854_13856del	NG_029581.1:g.13855_13856del	NG_029581.1:g.13856del	NG_029581.1:g.13856dup	NG_029581.1:g.13841_13856A[28]GAAA[2]A[14]	NG_029581.1:g.13841_13856A[19]GAAAAAAAA[2]A[9]	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[29]GAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[18]GAAAAAAAAACAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[19]GAAAAAAAAACAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13855_13856dup	NG_029581.1:g.13841_13856A[28]GAAA[2]A[15]	NG_029581.1:g.13841_13856A[17]GAAAAAAAA[2]A[10]	NG_029581.1:g.13841_13856A[19]GAAAAAAAA[2]A[10]	NG_029581.1:g.13841_13856A[27]GAAAAAAAA[2]A[10]	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13854_13856dup	NG_029581.1:g.13853_13856dup	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[28]GAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13848_13856dup	NG_029581.1:g.13847_13856dup	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13846_13856dup	NG_029581.1:g.13841_13856A[17]GAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13845_13856dup	NG_029581.1:g.13841_13856A[20]GAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13844_13856dup	NG_029581.1:g.13841_13856A[18]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAA	NG_029581.1:g.13841_13856A[19]GAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAA	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_029581.1:g.13856_13857insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CCDC39 transcript	NM_181426.1:c.91-6654=	NM_181426.1:c.91-6660_91-6654del	NM_181426.1:c.91-6659_91-6654del	NM_181426.1:c.91-6657_91-6654del	NM_181426.1:c.91-6656_91-6654del	NM_181426.1:c.91-6655_91-6654del	NM_181426.1:c.91-6654del	NM_181426.1:c.91-6654dup	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAGA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAGA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAACA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAACA	NM_181426.1:c.91-6655_91-6654dup	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAAAAAAAAGAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAGAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAGAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAA	NM_181426.1:c.91-6656_91-6654dup	NM_181426.1:c.91-6657_91-6654dup	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAA	NM_181426.1:c.91-6662_91-6654dup	NM_181426.1:c.91-6663_91-6654dup	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAAA	NM_181426.1:c.91-6664_91-6654dup	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAA	NM_181426.1:c.91-6665_91-6654dup	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA	NM_181426.1:c.91-6666_91-6654dup	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.1:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
CCDC39 transcript	NM_181426.2:c.91-6654=	NM_181426.2:c.91-6660_91-6654del	NM_181426.2:c.91-6659_91-6654del	NM_181426.2:c.91-6657_91-6654del	NM_181426.2:c.91-6656_91-6654del	NM_181426.2:c.91-6655_91-6654del	NM_181426.2:c.91-6654del	NM_181426.2:c.91-6654dup	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAGA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAGA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAACA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAACA	NM_181426.2:c.91-6655_91-6654dup	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAGAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAAAAAAAAGAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAGAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAGAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAA	NM_181426.2:c.91-6656_91-6654dup	NM_181426.2:c.91-6657_91-6654dup	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAA	NM_181426.2:c.91-6662_91-6654dup	NM_181426.2:c.91-6663_91-6654dup	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAAA	NM_181426.2:c.91-6664_91-6654dup	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAGAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAA	NM_181426.2:c.91-6665_91-6654dup	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA	NM_181426.2:c.91-6666_91-6654dup	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_181426.2:c.91-6654_91-6653insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

86 SubSNP, 67 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80897599	Oct 12, 2018 (152)
2	HGSV	ss83493585	Oct 12, 2018 (152)
3	HGSV	ss83582004	Oct 12, 2018 (152)
4	HUMANGENOME_JCVI	ss95970526	Oct 12, 2018 (152)
5	GMI	ss288457019	Oct 12, 2018 (152)
6	1000GENOMES	ss1371432771	Aug 21, 2014 (142)
7	EVA_GENOME_DK	ss1576109519	Apr 01, 2015 (144)
8	HAMMER_LAB	ss1800537292	Sep 08, 2015 (146)
9	SWEGEN	ss2993743251	Nov 08, 2017 (151)
10	URBANLAB	ss3647599287	Oct 12, 2018 (152)
11	EVA_DECODE	ss3710948956	Jul 13, 2019 (153)
12	EVA_DECODE	ss3710948958	Jul 13, 2019 (153)
13	EVA_DECODE	ss3710948959	Jul 13, 2019 (153)
14	EVA_DECODE	ss3710948960	Jul 13, 2019 (153)
15	ACPOP	ss3730648420	Jul 13, 2019 (153)
16	ACPOP	ss3730648421	Jul 13, 2019 (153)
17	PACBIO	ss3784553175	Jul 13, 2019 (153)
18	KHV_HUMAN_GENOMES	ss3804248066	Jul 13, 2019 (153)
19	EVA	ss3828249658	Apr 25, 2020 (154)
20	EVA	ss3837557131	Apr 25, 2020 (154)
21	EVA	ss3842989539	Apr 25, 2020 (154)
22	KOGIC	ss3953060599	Apr 25, 2020 (154)
23	KOGIC	ss3953060600	Apr 25, 2020 (154)
24	KOGIC	ss3953060601	Apr 25, 2020 (154)
25	KOGIC	ss3953060602	Apr 25, 2020 (154)
26	KOGIC	ss3953060603	Apr 25, 2020 (154)
27	GNOMAD	ss4086801050	Apr 26, 2021 (155)
28	GNOMAD	ss4086801052	Apr 26, 2021 (155)
29	GNOMAD	ss4086801053	Apr 26, 2021 (155)
30	GNOMAD	ss4086801054	Apr 26, 2021 (155)
31	GNOMAD	ss4086801055	Apr 26, 2021 (155)
32	GNOMAD	ss4086801056	Apr 26, 2021 (155)
33	GNOMAD	ss4086801057	Apr 26, 2021 (155)
34	GNOMAD	ss4086801058	Apr 26, 2021 (155)
35	GNOMAD	ss4086801059	Apr 26, 2021 (155)
36	GNOMAD	ss4086801061	Apr 26, 2021 (155)
37	GNOMAD	ss4086801062	Apr 26, 2021 (155)
38	GNOMAD	ss4086801063	Apr 26, 2021 (155)
39	GNOMAD	ss4086801064	Apr 26, 2021 (155)
40	GNOMAD	ss4086801065	Apr 26, 2021 (155)
41	GNOMAD	ss4086801066	Apr 26, 2021 (155)
42	GNOMAD	ss4086801067	Apr 26, 2021 (155)
43	GNOMAD	ss4086801068	Apr 26, 2021 (155)
44	GNOMAD	ss4086801069	Apr 26, 2021 (155)
45	GNOMAD	ss4086801070	Apr 26, 2021 (155)
46	GNOMAD	ss4086801071	Apr 26, 2021 (155)
47	GNOMAD	ss4086801072	Apr 26, 2021 (155)
48	GNOMAD	ss4086801073	Apr 26, 2021 (155)
49	GNOMAD	ss4086801074	Apr 26, 2021 (155)
50	GNOMAD	ss4086801075	Apr 26, 2021 (155)
51	GNOMAD	ss4086801076	Apr 26, 2021 (155)
52	GNOMAD	ss4086801077	Apr 26, 2021 (155)
53	GNOMAD	ss4086801078	Apr 26, 2021 (155)
54	GNOMAD	ss4086801079	Apr 26, 2021 (155)
55	GNOMAD	ss4086801080	Apr 26, 2021 (155)
56	GNOMAD	ss4086801081	Apr 26, 2021 (155)
57	GNOMAD	ss4086801082	Apr 26, 2021 (155)
58	GNOMAD	ss4086801083	Apr 26, 2021 (155)
59	GNOMAD	ss4086801084	Apr 26, 2021 (155)
60	GNOMAD	ss4086801085	Apr 26, 2021 (155)
61	GNOMAD	ss4086801086	Apr 26, 2021 (155)
62	GNOMAD	ss4086801087	Apr 26, 2021 (155)
63	GNOMAD	ss4086801088	Apr 26, 2021 (155)
64	GNOMAD	ss4086801089	Apr 26, 2021 (155)
65	GNOMAD	ss4086801090	Apr 26, 2021 (155)
66	GNOMAD	ss4086801091	Apr 26, 2021 (155)
67	GNOMAD	ss4086801092	Apr 26, 2021 (155)
68	GNOMAD	ss4086801093	Apr 26, 2021 (155)
69	GNOMAD	ss4086801094	Apr 26, 2021 (155)
70	GNOMAD	ss4086801095	Apr 26, 2021 (155)
71	GNOMAD	ss4086801096	Apr 26, 2021 (155)
72	GNOMAD	ss4086801097	Apr 26, 2021 (155)
73	GNOMAD	ss4086801098	Apr 26, 2021 (155)
74	TOPMED	ss4595565665	Apr 26, 2021 (155)
75	TOMMO_GENOMICS	ss5163125152	Apr 26, 2021 (155)
76	TOMMO_GENOMICS	ss5163125153	Apr 26, 2021 (155)
77	TOMMO_GENOMICS	ss5163125154	Apr 26, 2021 (155)
78	TOMMO_GENOMICS	ss5163125155	Apr 26, 2021 (155)
79	1000G_HIGH_COVERAGE	ss5257221838	Oct 13, 2022 (156)
80	1000G_HIGH_COVERAGE	ss5257221839	Oct 13, 2022 (156)
81	TOMMO_GENOMICS	ss5696444155	Oct 13, 2022 (156)
82	TOMMO_GENOMICS	ss5696444157	Oct 13, 2022 (156)
83	TOMMO_GENOMICS	ss5696444158	Oct 13, 2022 (156)
84	TOMMO_GENOMICS	ss5696444159	Oct 13, 2022 (156)
85	TOMMO_GENOMICS	ss5696444160	Oct 13, 2022 (156)
86	EVA	ss5853984492	Oct 13, 2022 (156)
87	1000Genomes	NC_000003.11 - 180388428	Oct 12, 2018 (152)
88	The Danish reference pan genome	NC_000003.11 - 180388428	Apr 25, 2020 (154)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
111	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
112	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
113	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
114	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
115	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
116	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
117	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
118	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
119	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
120	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
121	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
122	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
123	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
124	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
125	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
126	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
127	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
128	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
129	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
130	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
131	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
132	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
133	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
134	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
135	gnomAD - Genomes Submission ignored due to conflicting rows: Row 133819999 (NC_000003.12:180670639::T 24786/110714) Row 133820001 (NC_000003.12:180670639::TT 612/110782) Row 133820002 (NC_000003.12:180670639::TTT 122/110802)...	-	Apr 26, 2021 (155)
136	Korean Genome Project Submission ignored due to conflicting rows: Row 9438600 (NC_000003.12:180670641::T 669/1828) Row 9438601 (NC_000003.12:180670640:T: 63/1828) Row 9438602 (NC_000003.12:180670641::TT 49/1828)...	-	Apr 25, 2020 (154)
137	Korean Genome Project Submission ignored due to conflicting rows: Row 9438600 (NC_000003.12:180670641::T 669/1828) Row 9438601 (NC_000003.12:180670640:T: 63/1828) Row 9438602 (NC_000003.12:180670641::TT 49/1828)...	-	Apr 25, 2020 (154)
138	Korean Genome Project Submission ignored due to conflicting rows: Row 9438600 (NC_000003.12:180670641::T 669/1828) Row 9438601 (NC_000003.12:180670640:T: 63/1828) Row 9438602 (NC_000003.12:180670641::TT 49/1828)...	-	Apr 25, 2020 (154)
139	Korean Genome Project Submission ignored due to conflicting rows: Row 9438600 (NC_000003.12:180670641::T 669/1828) Row 9438601 (NC_000003.12:180670640:T: 63/1828) Row 9438602 (NC_000003.12:180670641::TT 49/1828)...	-	Apr 25, 2020 (154)
140	Korean Genome Project Submission ignored due to conflicting rows: Row 9438600 (NC_000003.12:180670641::T 669/1828) Row 9438601 (NC_000003.12:180670640:T: 63/1828) Row 9438602 (NC_000003.12:180670641::TT 49/1828)...	-	Apr 25, 2020 (154)
141	Northern Sweden Submission ignored due to conflicting rows: Row 3933285 (NC_000003.11:180388427::T 47/596) Row 3933286 (NC_000003.11:180388427::TTTTTTTTTTTT 8/596)	-	Jul 13, 2019 (153)
142	Northern Sweden Submission ignored due to conflicting rows: Row 3933285 (NC_000003.11:180388427::T 47/596) Row 3933286 (NC_000003.11:180388427::TTTTTTTTTTTT 8/596)	-	Jul 13, 2019 (153)
143	8.3KJPN Submission ignored due to conflicting rows: Row 21094459 (NC_000003.11:180388427::T 4620/16550) Row 21094460 (NC_000003.11:180388427::TT 357/16550) Row 21094461 (NC_000003.11:180388427:T: 37/16550)...	-	Apr 26, 2021 (155)
144	8.3KJPN Submission ignored due to conflicting rows: Row 21094459 (NC_000003.11:180388427::T 4620/16550) Row 21094460 (NC_000003.11:180388427::TT 357/16550) Row 21094461 (NC_000003.11:180388427:T: 37/16550)...	-	Apr 26, 2021 (155)
145	8.3KJPN Submission ignored due to conflicting rows: Row 21094459 (NC_000003.11:180388427::T 4620/16550) Row 21094460 (NC_000003.11:180388427::TT 357/16550) Row 21094461 (NC_000003.11:180388427:T: 37/16550)...	-	Apr 26, 2021 (155)
146	8.3KJPN Submission ignored due to conflicting rows: Row 21094459 (NC_000003.11:180388427::T 4620/16550) Row 21094460 (NC_000003.11:180388427::TT 357/16550) Row 21094461 (NC_000003.11:180388427:T: 37/16550)...	-	Apr 26, 2021 (155)
147	14KJPN Submission ignored due to conflicting rows: Row 30281259 (NC_000003.12:180670639::T 8293/28244) Row 30281261 (NC_000003.12:180670639::TT 681/28244) Row 30281262 (NC_000003.12:180670639:T: 71/28244)...	-	Oct 13, 2022 (156)
148	14KJPN Submission ignored due to conflicting rows: Row 30281259 (NC_000003.12:180670639::T 8293/28244) Row 30281261 (NC_000003.12:180670639::TT 681/28244) Row 30281262 (NC_000003.12:180670639:T: 71/28244)...	-	Oct 13, 2022 (156)
149	14KJPN Submission ignored due to conflicting rows: Row 30281259 (NC_000003.12:180670639::T 8293/28244) Row 30281261 (NC_000003.12:180670639::TT 681/28244) Row 30281262 (NC_000003.12:180670639:T: 71/28244)...	-	Oct 13, 2022 (156)
150	14KJPN Submission ignored due to conflicting rows: Row 30281259 (NC_000003.12:180670639::T 8293/28244) Row 30281261 (NC_000003.12:180670639::TT 681/28244) Row 30281262 (NC_000003.12:180670639:T: 71/28244)...	-	Oct 13, 2022 (156)
151	14KJPN Submission ignored due to conflicting rows: Row 30281259 (NC_000003.12:180670639::T 8293/28244) Row 30281261 (NC_000003.12:180670639::TT 681/28244) Row 30281262 (NC_000003.12:180670639:T: 71/28244)...	-	Oct 13, 2022 (156)
152	TopMed	NC_000003.12 - 180670640	Apr 26, 2021 (155)
153	ALFA	NC_000003.12 - 180670640	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).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss4086801098	NC_000003.12:180670639:TTTTTTT:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTT	(self)
432943220, ss4595565665	NC_000003.12:180670639:TTTTTT:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
ss4086801097	NC_000003.12:180670639:TTTT:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
ss4086801096	NC_000003.12:180670639:TTT:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss3710948956, ss3953060603, ss4086801095, ss5257221839	NC_000003.12:180670639:TT:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss1800537292, ss2993743251, ss3784553175, ss5163125154	NC_000003.11:180388427:T:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4086801094, ss5696444158	NC_000003.12:180670639:T:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss3710948958, ss3953060600	NC_000003.12:180670640:T:	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss288457019	NC_000003.10:181871137::T	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
18839974, 877687, ss1371432771, ss1576109519, ss3730648420, ss3828249658, ss3837557131, ss5163125152	NC_000003.11:180388427::T	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3647599287, ss3804248066, ss3842989539, ss4086801050, ss5257221838, ss5696444155, ss5853984492	NC_000003.12:180670639::T	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss3710948959, ss3953060599	NC_000003.12:180670641::T	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss80897599, ss83493585, ss83582004, ss95970526	NT_005612.16:86883589::T	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss4086801063	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801064	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTCTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4086801061	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTCT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTT	(self)
ss4086801062	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTCTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT	(self)
ss4086801065	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTCTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801066	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTGTTTTTTTTTCTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTCTTTTTTTTTTTTTTTTTT	(self)
ss4086801067	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTGTTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTGTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss5163125153	NC_000003.11:180388427::TT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4086801052, ss5696444157	NC_000003.12:180670639::TT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3710948960, ss3953060601	NC_000003.12:180670641::TT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss4086801070	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801071	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTCTTTTTTTTCT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTT	(self)
ss4086801072	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTCTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4086801073	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801068	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTCT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTT	(self)
ss4086801069	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss5163125155	NC_000003.11:180388427::TTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4086801053, ss5696444159	NC_000003.12:180670639::TTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3953060602	NC_000003.12:180670641::TTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss4086801054	NC_000003.12:180670639::TTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss4086801075	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTCTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT	(self)
ss4086801076	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTCTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT	(self)
ss4086801077	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4086801078	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801055	NC_000003.12:180670639::TTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801056	NC_000003.12:180670639::TTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801080	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTCT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTT	(self)
ss4086801081	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTCTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT	(self)
ss4086801082	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4086801057	NC_000003.12:180670639::TTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801083	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTCT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTT	(self)
ss4086801084	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTCTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT	(self)
ss4086801085	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss3730648421	NC_000003.11:180388427::TTTTTTTTTT… NC_000003.11:180388427::TTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801058, ss5696444160	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801086	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801059	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
6360139674	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801089	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTT	(self)
ss4086801074	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801090	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4086801079	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801087	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801088	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801091	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801092	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4086801093	NC_000003.12:180670639::TTTTTTTTTT… NC_000003.12:180670639::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000003.12:180670639:TTTTTTTTTTT… NC_000003.12:180670639:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

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

No publications for rs573623299

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

rs573623299