Name: rs34483652
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.

rs34483652

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr7:107558915-107558935 (GRCh38.p14) Help
The anchor position for this RefSNP. Includes all nucleotides potentially affected by this change, thus it can differ from HGVS, which is right-shifted. See here for details.
Alleles: del(A)₁₁ / del(A)₉ / del(A)₇ / del…
del(A)₁₁ / del(A)₉ / del(A)₇ / del(A)₆ / del(A)₅ / del(A)₄ / delAAA / delAA / delA / dupA / dupAA / dupAAA / dup(A)₄ / dup(A)₅ / dup(A)₆ / dup(A)₇ / dup(A)₈ / dup(A)₁₀ / dup(A)₁₁ / ins(A)₃₆ / insAAC(A)₄CC(A)₂₄ / insAC(A)₂₄
Variation Type: Indel Insertion and Deletion
Frequency: del(A)₁₁=0.0000 (0/9310, ALFA)
del(A)₉=0.0000 (0/9310, ALFA)
del(A)₇=0.0000 (0/9310, ALFA) (+ 9 more)
del(A)₆=0.0000 (0/9310, ALFA)
del(A)₅=0.0000 (0/9310, ALFA)
del(A)₄=0.0000 (0/9310, ALFA)
delAAA=0.0000 (0/9310, ALFA)
delAA=0.0000 (0/9310, ALFA)
delA=0.0000 (0/9310, ALFA)
dupA=0.0000 (0/9310, ALFA)
dupAA=0.0000 (0/9310, ALFA)
dupAAA=0.0000 (0/9310, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: COG5 : 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	9310	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
European	Sub	7470	AAAAAAAAAAAAAAAAAAAAA=1.0000	AAAAAAAAAA=0.0000, AAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAA=0.0000, AAAAAAAAAAAAAAAAAAAAAAAA=0.0000	1.0	N/A
African	Sub	690	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
African Others	Sub	12	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
African American	Sub	678	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Asian	Sub	86	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
East Asian	Sub	64	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other Asian	Sub	22	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Latin American 1	Sub	108	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
Latin American 2	Sub	536	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=0.000	1.0	N/A
South Asian	Sub	86	AAAAAAAAAAAAAAAAAAAAA=1.00	AAAAAAAAAA=0.00, AAAAAAAAAAAA=0.00, AAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAA=0.00, AAAAAAAAAAAAAAAAAAAAAAAA=0.00	1.0	N/A
Other	Sub	334	AAAAAAAAAAAAAAAAAAAAA=1.000	AAAAAAAAAA=0.000, AAAAAAAAAAAA=0.000, AAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAA=0.000, AAAAAAAAAAAAAAAAAAAAAAAA=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").

Download

Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	9310	(A)₂₁=1.0000	del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	European	Sub	7470	(A)₂₁=1.0000	del(A)₁₁=0.0000, del(A)₉=0.0000, del(A)₇=0.0000, del(A)₆=0.0000, del(A)₅=0.0000, del(A)₄=0.0000, delAAA=0.0000, delAA=0.0000, delA=0.0000, dupA=0.0000, dupAA=0.0000, dupAAA=0.0000
Allele Frequency Aggregator	African	Sub	690	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 2	Sub	536	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Other	Sub	334	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	Latin American 1	Sub	108	(A)₂₁=1.000	del(A)₁₁=0.000, del(A)₉=0.000, del(A)₇=0.000, del(A)₆=0.000, del(A)₅=0.000, del(A)₄=0.000, delAAA=0.000, delAA=0.000, delA=0.000, dupA=0.000, dupAA=0.000, dupAAA=0.000
Allele Frequency Aggregator	South Asian	Sub	86	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00
Allele Frequency Aggregator	Asian	Sub	86	(A)₂₁=1.00	del(A)₁₁=0.00, del(A)₉=0.00, del(A)₇=0.00, del(A)₆=0.00, del(A)₅=0.00, del(A)₄=0.00, delAAA=0.00, delAA=0.00, delA=0.00, dupA=0.00, dupAA=0.00, dupAAA=0.00

Variant Details tab shows known variant placements on genomic sequences: chromosomes (NC_), RefSeqGene, pseudogenes or genomic regions (NG_), and in a separate table: on transcripts (NM_) and protein sequences (NP_). The corresponding transcript and protein locations are listed in adjacent lines, along with molecular consequences from Sequence Ontology. When no protein placement is available, only the transcript is listed. Column "Codon[Amino acid]" shows the actual base change in the format of "Reference > Alternate" allele, including the nucleotide codon change in transcripts, and the amino acid change in proteins, respectively, allowing for known ribosomal slippage sites. To view nucleotides adjacent to the variant use the Genomic View at the bottom of the page - zoom into the sequence until the nucleotides around the variant become visible.

Genomic Placements

Sequence name	Change
GRCh38.p14 chr 7	NC_000007.14:g.107558925_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558927_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558929_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558930_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558931_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558932_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558933_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558934_107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558935del
GRCh38.p14 chr 7	NC_000007.14:g.107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558934_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558933_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558932_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558931_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558930_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558929_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558928_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558926_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558925_107558935dup
GRCh38.p14 chr 7	NC_000007.14:g.107558935_107558936insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 7	NC_000007.14:g.107558915_107558935A[23]CAAAACCAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 7	NC_000007.14:g.107558915_107558935A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 7	NC_000007.13:g.107199370_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199372_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199374_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199375_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199376_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199377_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199378_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199379_107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199380del
GRCh37.p13 chr 7	NC_000007.13:g.107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199379_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199378_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199377_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199376_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199375_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199374_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199373_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199371_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199370_107199380dup
GRCh37.p13 chr 7	NC_000007.13:g.107199380_107199381insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh37.p13 chr 7	NC_000007.13:g.107199360_107199380A[23]CAAAACCAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 7	NC_000007.13:g.107199360_107199380A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]
COG5 RefSeqGene	NG_028095.2:g.10590_10600del
COG5 RefSeqGene	NG_028095.2:g.10592_10600del
COG5 RefSeqGene	NG_028095.2:g.10594_10600del
COG5 RefSeqGene	NG_028095.2:g.10595_10600del
COG5 RefSeqGene	NG_028095.2:g.10596_10600del
COG5 RefSeqGene	NG_028095.2:g.10597_10600del
COG5 RefSeqGene	NG_028095.2:g.10598_10600del
COG5 RefSeqGene	NG_028095.2:g.10599_10600del
COG5 RefSeqGene	NG_028095.2:g.10600del
COG5 RefSeqGene	NG_028095.2:g.10600dup
COG5 RefSeqGene	NG_028095.2:g.10599_10600dup
COG5 RefSeqGene	NG_028095.2:g.10598_10600dup
COG5 RefSeqGene	NG_028095.2:g.10597_10600dup
COG5 RefSeqGene	NG_028095.2:g.10596_10600dup
COG5 RefSeqGene	NG_028095.2:g.10595_10600dup
COG5 RefSeqGene	NG_028095.2:g.10594_10600dup
COG5 RefSeqGene	NG_028095.2:g.10593_10600dup
COG5 RefSeqGene	NG_028095.2:g.10591_10600dup
COG5 RefSeqGene	NG_028095.2:g.10590_10600dup
COG5 RefSeqGene	NG_028095.2:g.10600_10601insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
COG5 RefSeqGene	NG_028095.2:g.10580_10600T[24]GGTTTTGTTTTTTTTTTTTTTTTTTTTTTT[1]
COG5 RefSeqGene	NG_028095.2:g.10580_10600T[24]GTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404580_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404582_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404584_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404585_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404586_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404587_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404588_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404589_404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404590del
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404589_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404588_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404587_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404586_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404585_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404584_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404583_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404581_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404580_404590dup
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404590_404591insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404570_404590A[23]CAAAACCAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404570_404590A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]

Gene: COG5, component of oligomeric golgi complex 5 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
COG5 transcript variant 3	NM_001161520.2:c.95-810_9… NM_001161520.2:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 4	NM_001379511.1:c.95-810_9… NM_001379511.1:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 5	NM_001379512.1:c.95-810_9… NM_001379512.1:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 6	NM_001379513.1:c.95-810_9… NM_001379513.1:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 7	NM_001379514.1:c.95-810_9… NM_001379514.1:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 8	NM_001379515.1:c.95-810_9… NM_001379515.1:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 9	NM_001379516.1:c.95-810_9… NM_001379516.1:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 1	NM_006348.5:c.95-810_95-8… NM_006348.5:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant 2	NM_181733.4:c.95-810_95-8… NM_181733.4:c.95-810_95-800del	N/A	Intron Variant
COG5 transcript variant X1	XM_024446634.2:c.95-810_9… XM_024446634.2:c.95-810_95-800del	N/A	Intron Variant

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

Not Reported in ClinVar

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

Placement	(A)₂₁=	del(A)₁₁	del(A)₉	del(A)₇	del(A)₆	del(A)₅	del(A)₄	delAAA	delAA	delA	dupA	dupAA	dupAAA	dup(A)₄	dup(A)₅	dup(A)₆	dup(A)₇	dup(A)₈	dup(A)₁₀	dup(A)₁₁	ins(A)₃₆	insAAC(A)₄CC(A)₂₄	insAC(A)₂₄
GRCh38.p14 chr 7	NC_000007.14:g.107558915_107558935=	NC_000007.14:g.107558925_107558935del	NC_000007.14:g.107558927_107558935del	NC_000007.14:g.107558929_107558935del	NC_000007.14:g.107558930_107558935del	NC_000007.14:g.107558931_107558935del	NC_000007.14:g.107558932_107558935del	NC_000007.14:g.107558933_107558935del	NC_000007.14:g.107558934_107558935del	NC_000007.14:g.107558935del	NC_000007.14:g.107558935dup	NC_000007.14:g.107558934_107558935dup	NC_000007.14:g.107558933_107558935dup	NC_000007.14:g.107558932_107558935dup	NC_000007.14:g.107558931_107558935dup	NC_000007.14:g.107558930_107558935dup	NC_000007.14:g.107558929_107558935dup	NC_000007.14:g.107558928_107558935dup	NC_000007.14:g.107558926_107558935dup	NC_000007.14:g.107558925_107558935dup	NC_000007.14:g.107558935_107558936insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:g.107558915_107558935A[23]CAAAACCAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000007.14:g.107558915_107558935A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]
GRCh37.p13 chr 7	NC_000007.13:g.107199360_107199380=	NC_000007.13:g.107199370_107199380del	NC_000007.13:g.107199372_107199380del	NC_000007.13:g.107199374_107199380del	NC_000007.13:g.107199375_107199380del	NC_000007.13:g.107199376_107199380del	NC_000007.13:g.107199377_107199380del	NC_000007.13:g.107199378_107199380del	NC_000007.13:g.107199379_107199380del	NC_000007.13:g.107199380del	NC_000007.13:g.107199380dup	NC_000007.13:g.107199379_107199380dup	NC_000007.13:g.107199378_107199380dup	NC_000007.13:g.107199377_107199380dup	NC_000007.13:g.107199376_107199380dup	NC_000007.13:g.107199375_107199380dup	NC_000007.13:g.107199374_107199380dup	NC_000007.13:g.107199373_107199380dup	NC_000007.13:g.107199371_107199380dup	NC_000007.13:g.107199370_107199380dup	NC_000007.13:g.107199380_107199381insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.13:g.107199360_107199380A[23]CAAAACCAAAAAAAAAAAAAAAAAAAAAAAA[1]	NC_000007.13:g.107199360_107199380A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]
COG5 RefSeqGene	NG_028095.2:g.10580_10600=	NG_028095.2:g.10590_10600del	NG_028095.2:g.10592_10600del	NG_028095.2:g.10594_10600del	NG_028095.2:g.10595_10600del	NG_028095.2:g.10596_10600del	NG_028095.2:g.10597_10600del	NG_028095.2:g.10598_10600del	NG_028095.2:g.10599_10600del	NG_028095.2:g.10600del	NG_028095.2:g.10600dup	NG_028095.2:g.10599_10600dup	NG_028095.2:g.10598_10600dup	NG_028095.2:g.10597_10600dup	NG_028095.2:g.10596_10600dup	NG_028095.2:g.10595_10600dup	NG_028095.2:g.10594_10600dup	NG_028095.2:g.10593_10600dup	NG_028095.2:g.10591_10600dup	NG_028095.2:g.10590_10600dup	NG_028095.2:g.10600_10601insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NG_028095.2:g.10580_10600T[24]GGTTTTGTTTTTTTTTTTTTTTTTTTTTTT[1]	NG_028095.2:g.10580_10600T[24]GTTTTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 7 fix patch HG2266_PATCH	NW_017852930.1:g.404570_404590=	NW_017852930.1:g.404580_404590del	NW_017852930.1:g.404582_404590del	NW_017852930.1:g.404584_404590del	NW_017852930.1:g.404585_404590del	NW_017852930.1:g.404586_404590del	NW_017852930.1:g.404587_404590del	NW_017852930.1:g.404588_404590del	NW_017852930.1:g.404589_404590del	NW_017852930.1:g.404590del	NW_017852930.1:g.404590dup	NW_017852930.1:g.404589_404590dup	NW_017852930.1:g.404588_404590dup	NW_017852930.1:g.404587_404590dup	NW_017852930.1:g.404586_404590dup	NW_017852930.1:g.404585_404590dup	NW_017852930.1:g.404584_404590dup	NW_017852930.1:g.404583_404590dup	NW_017852930.1:g.404581_404590dup	NW_017852930.1:g.404580_404590dup	NW_017852930.1:g.404590_404591insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NW_017852930.1:g.404570_404590A[23]CAAAACCAAAAAAAAAAAAAAAAAAAAAAAA[1]	NW_017852930.1:g.404570_404590A[22]CAAAAAAAAAAAAAAAAAAAAAAAA[1]
COG5 transcript variant 3	NM_001161520.1:c.188-800=	NM_001161520.1:c.188-810_188-800del	NM_001161520.1:c.188-808_188-800del	NM_001161520.1:c.188-806_188-800del	NM_001161520.1:c.188-805_188-800del	NM_001161520.1:c.188-804_188-800del	NM_001161520.1:c.188-803_188-800del	NM_001161520.1:c.188-802_188-800del	NM_001161520.1:c.188-801_188-800del	NM_001161520.1:c.188-800del	NM_001161520.1:c.188-800dup	NM_001161520.1:c.188-801_188-800dup	NM_001161520.1:c.188-802_188-800dup	NM_001161520.1:c.188-803_188-800dup	NM_001161520.1:c.188-804_188-800dup	NM_001161520.1:c.188-805_188-800dup	NM_001161520.1:c.188-806_188-800dup	NM_001161520.1:c.188-807_188-800dup	NM_001161520.1:c.188-809_188-800dup	NM_001161520.1:c.188-810_188-800dup	NM_001161520.1:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001161520.1:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001161520.1:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 3	NM_001161520.2:c.95-800=	NM_001161520.2:c.95-810_95-800del	NM_001161520.2:c.95-808_95-800del	NM_001161520.2:c.95-806_95-800del	NM_001161520.2:c.95-805_95-800del	NM_001161520.2:c.95-804_95-800del	NM_001161520.2:c.95-803_95-800del	NM_001161520.2:c.95-802_95-800del	NM_001161520.2:c.95-801_95-800del	NM_001161520.2:c.95-800del	NM_001161520.2:c.95-800dup	NM_001161520.2:c.95-801_95-800dup	NM_001161520.2:c.95-802_95-800dup	NM_001161520.2:c.95-803_95-800dup	NM_001161520.2:c.95-804_95-800dup	NM_001161520.2:c.95-805_95-800dup	NM_001161520.2:c.95-806_95-800dup	NM_001161520.2:c.95-807_95-800dup	NM_001161520.2:c.95-809_95-800dup	NM_001161520.2:c.95-810_95-800dup	NM_001161520.2:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001161520.2:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001161520.2:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 4	NM_001379511.1:c.95-800=	NM_001379511.1:c.95-810_95-800del	NM_001379511.1:c.95-808_95-800del	NM_001379511.1:c.95-806_95-800del	NM_001379511.1:c.95-805_95-800del	NM_001379511.1:c.95-804_95-800del	NM_001379511.1:c.95-803_95-800del	NM_001379511.1:c.95-802_95-800del	NM_001379511.1:c.95-801_95-800del	NM_001379511.1:c.95-800del	NM_001379511.1:c.95-800dup	NM_001379511.1:c.95-801_95-800dup	NM_001379511.1:c.95-802_95-800dup	NM_001379511.1:c.95-803_95-800dup	NM_001379511.1:c.95-804_95-800dup	NM_001379511.1:c.95-805_95-800dup	NM_001379511.1:c.95-806_95-800dup	NM_001379511.1:c.95-807_95-800dup	NM_001379511.1:c.95-809_95-800dup	NM_001379511.1:c.95-810_95-800dup	NM_001379511.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001379511.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001379511.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 5	NM_001379512.1:c.95-800=	NM_001379512.1:c.95-810_95-800del	NM_001379512.1:c.95-808_95-800del	NM_001379512.1:c.95-806_95-800del	NM_001379512.1:c.95-805_95-800del	NM_001379512.1:c.95-804_95-800del	NM_001379512.1:c.95-803_95-800del	NM_001379512.1:c.95-802_95-800del	NM_001379512.1:c.95-801_95-800del	NM_001379512.1:c.95-800del	NM_001379512.1:c.95-800dup	NM_001379512.1:c.95-801_95-800dup	NM_001379512.1:c.95-802_95-800dup	NM_001379512.1:c.95-803_95-800dup	NM_001379512.1:c.95-804_95-800dup	NM_001379512.1:c.95-805_95-800dup	NM_001379512.1:c.95-806_95-800dup	NM_001379512.1:c.95-807_95-800dup	NM_001379512.1:c.95-809_95-800dup	NM_001379512.1:c.95-810_95-800dup	NM_001379512.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001379512.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001379512.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 6	NM_001379513.1:c.95-800=	NM_001379513.1:c.95-810_95-800del	NM_001379513.1:c.95-808_95-800del	NM_001379513.1:c.95-806_95-800del	NM_001379513.1:c.95-805_95-800del	NM_001379513.1:c.95-804_95-800del	NM_001379513.1:c.95-803_95-800del	NM_001379513.1:c.95-802_95-800del	NM_001379513.1:c.95-801_95-800del	NM_001379513.1:c.95-800del	NM_001379513.1:c.95-800dup	NM_001379513.1:c.95-801_95-800dup	NM_001379513.1:c.95-802_95-800dup	NM_001379513.1:c.95-803_95-800dup	NM_001379513.1:c.95-804_95-800dup	NM_001379513.1:c.95-805_95-800dup	NM_001379513.1:c.95-806_95-800dup	NM_001379513.1:c.95-807_95-800dup	NM_001379513.1:c.95-809_95-800dup	NM_001379513.1:c.95-810_95-800dup	NM_001379513.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001379513.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001379513.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 7	NM_001379514.1:c.95-800=	NM_001379514.1:c.95-810_95-800del	NM_001379514.1:c.95-808_95-800del	NM_001379514.1:c.95-806_95-800del	NM_001379514.1:c.95-805_95-800del	NM_001379514.1:c.95-804_95-800del	NM_001379514.1:c.95-803_95-800del	NM_001379514.1:c.95-802_95-800del	NM_001379514.1:c.95-801_95-800del	NM_001379514.1:c.95-800del	NM_001379514.1:c.95-800dup	NM_001379514.1:c.95-801_95-800dup	NM_001379514.1:c.95-802_95-800dup	NM_001379514.1:c.95-803_95-800dup	NM_001379514.1:c.95-804_95-800dup	NM_001379514.1:c.95-805_95-800dup	NM_001379514.1:c.95-806_95-800dup	NM_001379514.1:c.95-807_95-800dup	NM_001379514.1:c.95-809_95-800dup	NM_001379514.1:c.95-810_95-800dup	NM_001379514.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001379514.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001379514.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 8	NM_001379515.1:c.95-800=	NM_001379515.1:c.95-810_95-800del	NM_001379515.1:c.95-808_95-800del	NM_001379515.1:c.95-806_95-800del	NM_001379515.1:c.95-805_95-800del	NM_001379515.1:c.95-804_95-800del	NM_001379515.1:c.95-803_95-800del	NM_001379515.1:c.95-802_95-800del	NM_001379515.1:c.95-801_95-800del	NM_001379515.1:c.95-800del	NM_001379515.1:c.95-800dup	NM_001379515.1:c.95-801_95-800dup	NM_001379515.1:c.95-802_95-800dup	NM_001379515.1:c.95-803_95-800dup	NM_001379515.1:c.95-804_95-800dup	NM_001379515.1:c.95-805_95-800dup	NM_001379515.1:c.95-806_95-800dup	NM_001379515.1:c.95-807_95-800dup	NM_001379515.1:c.95-809_95-800dup	NM_001379515.1:c.95-810_95-800dup	NM_001379515.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001379515.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001379515.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 9	NM_001379516.1:c.95-800=	NM_001379516.1:c.95-810_95-800del	NM_001379516.1:c.95-808_95-800del	NM_001379516.1:c.95-806_95-800del	NM_001379516.1:c.95-805_95-800del	NM_001379516.1:c.95-804_95-800del	NM_001379516.1:c.95-803_95-800del	NM_001379516.1:c.95-802_95-800del	NM_001379516.1:c.95-801_95-800del	NM_001379516.1:c.95-800del	NM_001379516.1:c.95-800dup	NM_001379516.1:c.95-801_95-800dup	NM_001379516.1:c.95-802_95-800dup	NM_001379516.1:c.95-803_95-800dup	NM_001379516.1:c.95-804_95-800dup	NM_001379516.1:c.95-805_95-800dup	NM_001379516.1:c.95-806_95-800dup	NM_001379516.1:c.95-807_95-800dup	NM_001379516.1:c.95-809_95-800dup	NM_001379516.1:c.95-810_95-800dup	NM_001379516.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_001379516.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_001379516.1:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 1	NM_006348.3:c.188-800=	NM_006348.3:c.188-810_188-800del	NM_006348.3:c.188-808_188-800del	NM_006348.3:c.188-806_188-800del	NM_006348.3:c.188-805_188-800del	NM_006348.3:c.188-804_188-800del	NM_006348.3:c.188-803_188-800del	NM_006348.3:c.188-802_188-800del	NM_006348.3:c.188-801_188-800del	NM_006348.3:c.188-800del	NM_006348.3:c.188-800dup	NM_006348.3:c.188-801_188-800dup	NM_006348.3:c.188-802_188-800dup	NM_006348.3:c.188-803_188-800dup	NM_006348.3:c.188-804_188-800dup	NM_006348.3:c.188-805_188-800dup	NM_006348.3:c.188-806_188-800dup	NM_006348.3:c.188-807_188-800dup	NM_006348.3:c.188-809_188-800dup	NM_006348.3:c.188-810_188-800dup	NM_006348.3:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_006348.3:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_006348.3:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 1	NM_006348.5:c.95-800=	NM_006348.5:c.95-810_95-800del	NM_006348.5:c.95-808_95-800del	NM_006348.5:c.95-806_95-800del	NM_006348.5:c.95-805_95-800del	NM_006348.5:c.95-804_95-800del	NM_006348.5:c.95-803_95-800del	NM_006348.5:c.95-802_95-800del	NM_006348.5:c.95-801_95-800del	NM_006348.5:c.95-800del	NM_006348.5:c.95-800dup	NM_006348.5:c.95-801_95-800dup	NM_006348.5:c.95-802_95-800dup	NM_006348.5:c.95-803_95-800dup	NM_006348.5:c.95-804_95-800dup	NM_006348.5:c.95-805_95-800dup	NM_006348.5:c.95-806_95-800dup	NM_006348.5:c.95-807_95-800dup	NM_006348.5:c.95-809_95-800dup	NM_006348.5:c.95-810_95-800dup	NM_006348.5:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_006348.5:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_006348.5:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 2	NM_181733.2:c.188-800=	NM_181733.2:c.188-810_188-800del	NM_181733.2:c.188-808_188-800del	NM_181733.2:c.188-806_188-800del	NM_181733.2:c.188-805_188-800del	NM_181733.2:c.188-804_188-800del	NM_181733.2:c.188-803_188-800del	NM_181733.2:c.188-802_188-800del	NM_181733.2:c.188-801_188-800del	NM_181733.2:c.188-800del	NM_181733.2:c.188-800dup	NM_181733.2:c.188-801_188-800dup	NM_181733.2:c.188-802_188-800dup	NM_181733.2:c.188-803_188-800dup	NM_181733.2:c.188-804_188-800dup	NM_181733.2:c.188-805_188-800dup	NM_181733.2:c.188-806_188-800dup	NM_181733.2:c.188-807_188-800dup	NM_181733.2:c.188-809_188-800dup	NM_181733.2:c.188-810_188-800dup	NM_181733.2:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_181733.2:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_181733.2:c.188-800_188-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant 2	NM_181733.4:c.95-800=	NM_181733.4:c.95-810_95-800del	NM_181733.4:c.95-808_95-800del	NM_181733.4:c.95-806_95-800del	NM_181733.4:c.95-805_95-800del	NM_181733.4:c.95-804_95-800del	NM_181733.4:c.95-803_95-800del	NM_181733.4:c.95-802_95-800del	NM_181733.4:c.95-801_95-800del	NM_181733.4:c.95-800del	NM_181733.4:c.95-800dup	NM_181733.4:c.95-801_95-800dup	NM_181733.4:c.95-802_95-800dup	NM_181733.4:c.95-803_95-800dup	NM_181733.4:c.95-804_95-800dup	NM_181733.4:c.95-805_95-800dup	NM_181733.4:c.95-806_95-800dup	NM_181733.4:c.95-807_95-800dup	NM_181733.4:c.95-809_95-800dup	NM_181733.4:c.95-810_95-800dup	NM_181733.4:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NM_181733.4:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	NM_181733.4:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT
COG5 transcript variant X1	XM_024446634.2:c.95-800=	XM_024446634.2:c.95-810_95-800del	XM_024446634.2:c.95-808_95-800del	XM_024446634.2:c.95-806_95-800del	XM_024446634.2:c.95-805_95-800del	XM_024446634.2:c.95-804_95-800del	XM_024446634.2:c.95-803_95-800del	XM_024446634.2:c.95-802_95-800del	XM_024446634.2:c.95-801_95-800del	XM_024446634.2:c.95-800del	XM_024446634.2:c.95-800dup	XM_024446634.2:c.95-801_95-800dup	XM_024446634.2:c.95-802_95-800dup	XM_024446634.2:c.95-803_95-800dup	XM_024446634.2:c.95-804_95-800dup	XM_024446634.2:c.95-805_95-800dup	XM_024446634.2:c.95-806_95-800dup	XM_024446634.2:c.95-807_95-800dup	XM_024446634.2:c.95-809_95-800dup	XM_024446634.2:c.95-810_95-800dup	XM_024446634.2:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XM_024446634.2:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGGTTTTGTT	XM_024446634.2:c.95-800_95-799insTTTTTTTTTTTTTTTTTTTTTTTTGT

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#.

44 SubSNP, 28 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	ABI	ss43015068	Mar 13, 2006 (126)
2	HGSV	ss82735337	Dec 14, 2007 (129)
3	EVA_DECODE	ss3720411783	Jul 13, 2019 (153)
4	EVA_DECODE	ss3720411784	Jul 13, 2019 (153)
5	EVA_DECODE	ss3720411785	Jul 13, 2019 (153)
6	EVA_DECODE	ss3720411786	Jul 13, 2019 (153)
7	EVA_DECODE	ss3720411787	Jul 13, 2019 (153)
8	EVA_DECODE	ss3720411788	Jul 13, 2019 (153)
9	PACBIO	ss3791205455	Jul 13, 2019 (153)
10	PACBIO	ss3796085544	Jul 13, 2019 (153)
11	GNOMAD	ss4170414369	Apr 26, 2021 (155)
12	GNOMAD	ss4170414370	Apr 26, 2021 (155)
13	GNOMAD	ss4170414371	Apr 26, 2021 (155)
14	GNOMAD	ss4170414372	Apr 26, 2021 (155)
15	GNOMAD	ss4170414373	Apr 26, 2021 (155)
16	GNOMAD	ss4170414374	Apr 26, 2021 (155)
17	GNOMAD	ss4170414375	Apr 26, 2021 (155)
18	GNOMAD	ss4170414376	Apr 26, 2021 (155)
19	GNOMAD	ss4170414377	Apr 26, 2021 (155)
20	GNOMAD	ss4170414378	Apr 26, 2021 (155)
21	GNOMAD	ss4170414379	Apr 26, 2021 (155)
22	GNOMAD	ss4170414380	Apr 26, 2021 (155)
23	GNOMAD	ss4170414381	Apr 26, 2021 (155)
24	GNOMAD	ss4170414384	Apr 26, 2021 (155)
25	GNOMAD	ss4170414385	Apr 26, 2021 (155)
26	GNOMAD	ss4170414386	Apr 26, 2021 (155)
27	GNOMAD	ss4170414387	Apr 26, 2021 (155)
28	GNOMAD	ss4170414388	Apr 26, 2021 (155)
29	TOMMO_GENOMICS	ss5184935140	Apr 26, 2021 (155)
30	TOMMO_GENOMICS	ss5184935141	Apr 26, 2021 (155)
31	TOMMO_GENOMICS	ss5184935142	Apr 26, 2021 (155)
32	TOMMO_GENOMICS	ss5184935143	Apr 26, 2021 (155)
33	TOMMO_GENOMICS	ss5184935144	Apr 26, 2021 (155)
34	1000G_HIGH_COVERAGE	ss5274233635	Oct 14, 2022 (156)
35	1000G_HIGH_COVERAGE	ss5274233636	Oct 14, 2022 (156)
36	1000G_HIGH_COVERAGE	ss5274233637	Oct 14, 2022 (156)
37	HUGCELL_USP	ss5471172115	Oct 14, 2022 (156)
38	HUGCELL_USP	ss5471172116	Oct 14, 2022 (156)
39	HUGCELL_USP	ss5471172117	Oct 14, 2022 (156)
40	HUGCELL_USP	ss5471172118	Oct 14, 2022 (156)
41	TOMMO_GENOMICS	ss5725738687	Oct 14, 2022 (156)
42	TOMMO_GENOMICS	ss5725738688	Oct 14, 2022 (156)
43	TOMMO_GENOMICS	ss5725738689	Oct 14, 2022 (156)
44	TOMMO_GENOMICS	ss5725738691	Oct 14, 2022 (156)
45	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
46	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
47	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
48	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
49	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
50	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
51	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
52	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
53	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
54	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
55	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
56	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
57	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
58	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
59	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
60	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
61	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
62	gnomAD - Genomes Submission ignored due to conflicting rows: Row 272290081 (NC_000007.14:107558914::A 1769/29962) Row 272290082 (NC_000007.14:107558914::AA 366/29922) Row 272290083 (NC_000007.14:107558914::AAA 42/29934)...	-	Apr 26, 2021 (155)
63	8.3KJPN Submission ignored due to conflicting rows: Row 42904447 (NC_000007.13:107199359::A 1613/15942) Row 42904448 (NC_000007.13:107199359:A: 207/15942) Row 42904449 (NC_000007.13:107199359:AA: 1146/15942)...	-	Apr 26, 2021 (155)
64	8.3KJPN Submission ignored due to conflicting rows: Row 42904447 (NC_000007.13:107199359::A 1613/15942) Row 42904448 (NC_000007.13:107199359:A: 207/15942) Row 42904449 (NC_000007.13:107199359:AA: 1146/15942)...	-	Apr 26, 2021 (155)
65	8.3KJPN Submission ignored due to conflicting rows: Row 42904447 (NC_000007.13:107199359::A 1613/15942) Row 42904448 (NC_000007.13:107199359:A: 207/15942) Row 42904449 (NC_000007.13:107199359:AA: 1146/15942)...	-	Apr 26, 2021 (155)
66	8.3KJPN Submission ignored due to conflicting rows: Row 42904447 (NC_000007.13:107199359::A 1613/15942) Row 42904448 (NC_000007.13:107199359:A: 207/15942) Row 42904449 (NC_000007.13:107199359:AA: 1146/15942)...	-	Apr 26, 2021 (155)
67	8.3KJPN Submission ignored due to conflicting rows: Row 42904447 (NC_000007.13:107199359::A 1613/15942) Row 42904448 (NC_000007.13:107199359:A: 207/15942) Row 42904449 (NC_000007.13:107199359:AA: 1146/15942)...	-	Apr 26, 2021 (155)
68	14KJPN Submission ignored due to conflicting rows: Row 59575791 (NC_000007.14:107558914::A 2441/25590) Row 59575792 (NC_000007.14:107558914:AA: 1738/25590) Row 59575793 (NC_000007.14:107558914:A: 322/25590)...	-	Oct 14, 2022 (156)
69	14KJPN Submission ignored due to conflicting rows: Row 59575791 (NC_000007.14:107558914::A 2441/25590) Row 59575792 (NC_000007.14:107558914:AA: 1738/25590) Row 59575793 (NC_000007.14:107558914:A: 322/25590)...	-	Oct 14, 2022 (156)
70	14KJPN Submission ignored due to conflicting rows: Row 59575791 (NC_000007.14:107558914::A 2441/25590) Row 59575792 (NC_000007.14:107558914:AA: 1738/25590) Row 59575793 (NC_000007.14:107558914:A: 322/25590)...	-	Oct 14, 2022 (156)
71	14KJPN Submission ignored due to conflicting rows: Row 59575791 (NC_000007.14:107558914::A 2441/25590) Row 59575792 (NC_000007.14:107558914:AA: 1738/25590) Row 59575793 (NC_000007.14:107558914:A: 322/25590)...	-	Oct 14, 2022 (156)
72	ALFA	NC_000007.14 - 107558915	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)
rs71699033	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA	(self)
ss4170414388	NC_000007.14:107558914:AAAAAAA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA	(self)
ss3720411788, ss4170414387	NC_000007.14:107558914:AAAA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA	(self)
ss5184935144	NC_000007.13:107199359:AAA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss4170414386, ss5274233637, ss5725738691	NC_000007.14:107558914:AAA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss3720411787	NC_000007.14:107558915:AAA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA	(self)
ss82735337	NC_000007.11:106793329:AA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss5184935142	NC_000007.13:107199359:AA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss4170414385, ss5274233635, ss5471172118, ss5725738688	NC_000007.14:107558914:AA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3720411786	NC_000007.14:107558916:AA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA	(self)
ss3791205455, ss3796085544, ss5184935141	NC_000007.13:107199359:A:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss4170414384, ss5471172115, ss5725738689	NC_000007.14:107558914:A:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss3720411785	NC_000007.14:107558917:A:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss43015068	NT_007933.15:45232204:A:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA	(self)
ss5184935140	NC_000007.13:107199359::A	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414369, ss5471172116, ss5725738687	NC_000007.14:107558914::A	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss3720411784	NC_000007.14:107558918::A	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA	(self)
ss5184935143	NC_000007.13:107199359::AA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414370, ss5274233636, ss5471172117	NC_000007.14:107558914::AA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss3720411783	NC_000007.14:107558918::AA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414371	NC_000007.14:107558914::AAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
910811797	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414372	NC_000007.14:107558914::AAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414373	NC_000007.14:107558914::AAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414374	NC_000007.14:107558914::AAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414375	NC_000007.14:107558914::AAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414376	NC_000007.14:107558914::AAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414377	NC_000007.14:107558914::AAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414378	NC_000007.14:107558914::AAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414379	NC_000007.14:107558914::AAAAAAAAAA… NC_000007.14:107558914::AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414380	NC_000007.14:107558914::AAAAAAAAAA… NC_000007.14:107558914::AAAAAAAAAAAAAAAAAAAAAAACAAAACCAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAACAAAACCAAAAAAAAAAAAAAAAAAAAAAAA	(self)
ss4170414381	NC_000007.14:107558914::AAAAAAAAAA… NC_000007.14:107558914::AAAAAAAAAAAAAAAAAAAAAACAAA	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3540511926	NC_000007.14:107558914:AAAAAA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA
ss3540511927	NC_000007.14:107558914:AAAAAAAAAAA:	NC_000007.14:107558914:AAAAAAAAAAA… NC_000007.14:107558914:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA

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

No publications for rs34483652

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

rs34483652