Name: rs59173874
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.

rs59173874

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr4:57103661-57103676 (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)₈ / del(T)₆ / del(T)₅ / del(…
del(T)₈ / del(T)₆ / del(T)₅ / del(T)₄ / delTTT / delTT / delT / dupT / dupTT / dupTTT / dup(T)₄ / dup(T)₅ / dup(T)₆ / dup(T)₇ / dup(T)₈ / dup(T)₉ / ins(T)₉C(T)₁₉ / dup(T)₁₀ / dup(T)₁₁ / dup(T)₁₂ / dup(T)₁₃ / dup(T)₁₅ / dup(T)₁₆ / ins(T)₁₇ / ins(T)₁₈ / ins(T)₁₉ / ins(T)₂₀ / ins(T)₂₁ / ins(T)₂₂ / ins(T)₂₃ / ins(T)₂₄ / ins(T)₂₅ / ins(T)₂₆ / ins(T)₂₇ / ins(T)₂₈ / ins(T)₂₉ / ins(T)₃₀ / ins(T)₃₂ / ins(T)₃₆
Variation Type: Indel Insertion and Deletion
Frequency: del(T)₈=0.000 (0/376, ALFA)
del(T)₆=0.000 (0/376, ALFA)
del(T)₅=0.000 (0/376, ALFA) (+ 11 more)
del(T)₄=0.000 (0/376, ALFA)
delTTT=0.000 (0/376, ALFA)
delTT=0.000 (0/376, ALFA)
delT=0.000 (0/376, ALFA)
dupT=0.000 (0/376, ALFA)
dupTT=0.000 (0/376, ALFA)
dupTTT=0.000 (0/376, ALFA)
dup(T)₄=0.000 (0/376, ALFA)
dup(T)₅=0.000 (0/376, ALFA)
dup(T)₆=0.000 (0/376, ALFA)
dup(T)₇=0.000 (0/376, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: IGFBP7 : 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	376	TTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
European	Sub	220	TTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African	Sub	132	TTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
African Others	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
African American	Sub	130	TTTTTTTTTTTTTTTT=1.000	TTTTTTTT=0.000, TTTTTTTTTT=0.000, TTTTTTTTTTT=0.000, TTTTTTTTTTTT=0.000, TTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTT=0.000, TTTTTTTTTTTTTTTTTTTTTTT=0.000	1.0	0.0	0.0	N/A
Asian	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
East Asian	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other Asian	Sub	0	TTTTTTTTTTTTTTTT=0	TTTTTTTT=0, TTTTTTTTTT=0, TTTTTTTTTTT=0, TTTTTTTTTTTT=0, TTTTTTTTTTTTT=0, TTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTT=0, TTTTTTTTTTTTTTTTTTTTTTT=0	0	0	0	N/A
Latin American 1	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Latin American 2	Sub	6	TTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
South Asian	Sub	2	TTTTTTTTTTTTTTTT=1.0	TTTTTTTT=0.0, TTTTTTTTTT=0.0, TTTTTTTTTTT=0.0, TTTTTTTTTTTT=0.0, TTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTT=0.0, TTTTTTTTTTTTTTTTTTTTTTT=0.0	1.0	0.0	0.0	N/A
Other	Sub	12	TTTTTTTTTTTTTTTT=1.00	TTTTTTTT=0.00, TTTTTTTTTT=0.00, TTTTTTTTTTT=0.00, TTTTTTTTTTTT=0.00, TTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTT=0.00, TTTTTTTTTTTTTTTTTTTTTTT=0.00	1.0	0.0	0.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	376	(T)₁₆=1.000	del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	European	Sub	220	(T)₁₆=1.000	del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	African	Sub	132	(T)₁₆=1.000	del(T)₈=0.000, del(T)₆=0.000, del(T)₅=0.000, del(T)₄=0.000, delTTT=0.000, delTT=0.000, delT=0.000, dupT=0.000, dupTT=0.000, dupTTT=0.000, dup(T)₄=0.000, dup(T)₅=0.000, dup(T)₆=0.000, dup(T)₇=0.000
Allele Frequency Aggregator	Other	Sub	12	(T)₁₆=1.00	del(T)₈=0.00, del(T)₆=0.00, del(T)₅=0.00, del(T)₄=0.00, delTTT=0.00, delTT=0.00, delT=0.00, dupT=0.00, dupTT=0.00, dupTTT=0.00, dup(T)₄=0.00, dup(T)₅=0.00, dup(T)₆=0.00, dup(T)₇=0.00
Allele Frequency Aggregator	Latin American 2	Sub	6	(T)₁₆=1.0	del(T)₈=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	Latin American 1	Sub	2	(T)₁₆=1.0	del(T)₈=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	South Asian	Sub	2	(T)₁₆=1.0	del(T)₈=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0
Allele Frequency Aggregator	Asian	Sub	2	(T)₁₆=1.0	del(T)₈=0.0, del(T)₆=0.0, del(T)₅=0.0, del(T)₄=0.0, delTTT=0.0, delTT=0.0, delT=0.0, dupT=0.0, dupTT=0.0, dupTTT=0.0, dup(T)₄=0.0, dup(T)₅=0.0, dup(T)₆=0.0, dup(T)₇=0.0

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 4	NC_000004.12:g.57103669_57103676del
GRCh38.p14 chr 4	NC_000004.12:g.57103671_57103676del
GRCh38.p14 chr 4	NC_000004.12:g.57103672_57103676del
GRCh38.p14 chr 4	NC_000004.12:g.57103673_57103676del
GRCh38.p14 chr 4	NC_000004.12:g.57103674_57103676del
GRCh38.p14 chr 4	NC_000004.12:g.57103675_57103676del
GRCh38.p14 chr 4	NC_000004.12:g.57103676del
GRCh38.p14 chr 4	NC_000004.12:g.57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103675_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103674_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103673_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103672_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103671_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103670_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103669_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103668_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103661_57103676T[25]CTTTTTTTTTTTTTTTTTTT[1]
GRCh38.p14 chr 4	NC_000004.12:g.57103667_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103666_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103665_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103664_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103662_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103661_57103676dup
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh38.p14 chr 4	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969835_57969842del
GRCh37.p13 chr 4	NC_000004.11:g.57969837_57969842del
GRCh37.p13 chr 4	NC_000004.11:g.57969838_57969842del
GRCh37.p13 chr 4	NC_000004.11:g.57969839_57969842del
GRCh37.p13 chr 4	NC_000004.11:g.57969840_57969842del
GRCh37.p13 chr 4	NC_000004.11:g.57969841_57969842del
GRCh37.p13 chr 4	NC_000004.11:g.57969842del
GRCh37.p13 chr 4	NC_000004.11:g.57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969841_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969840_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969839_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969838_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969837_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969836_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969835_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969834_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969827_57969842T[25]CTTTTTTTTTTTTTTTTTTT[1]
GRCh37.p13 chr 4	NC_000004.11:g.57969833_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969832_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969831_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969830_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969828_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969827_57969842dup
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
IGFBP7 RefSeqGene	NG_031877.1:g.11718_11725del
IGFBP7 RefSeqGene	NG_031877.1:g.11720_11725del
IGFBP7 RefSeqGene	NG_031877.1:g.11721_11725del
IGFBP7 RefSeqGene	NG_031877.1:g.11722_11725del
IGFBP7 RefSeqGene	NG_031877.1:g.11723_11725del
IGFBP7 RefSeqGene	NG_031877.1:g.11724_11725del
IGFBP7 RefSeqGene	NG_031877.1:g.11725del
IGFBP7 RefSeqGene	NG_031877.1:g.11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11724_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11723_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11722_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11721_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11720_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11719_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11718_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11717_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11710_11725A[19]GAAAAAAAAAAAAAAAAAAAAAAAAA[1]
IGFBP7 RefSeqGene	NG_031877.1:g.11716_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11715_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11714_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11713_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11711_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11710_11725dup
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 RefSeqGene	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Gene: IGFBP7, insulin like growth factor binding protein 7 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
IGFBP7 transcript variant 2	NM_001253835.2:c.475+6209… NM_001253835.2:c.475+6209_475+6216del	N/A	Intron Variant
IGFBP7 transcript variant 1	NM_001553.3:c.475+6209_47… NM_001553.3:c.475+6209_475+6216del	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)₈	del(T)₆	del(T)₅	del(T)₄	delTTT	delTT	delT	dupT	dupTT	dupTTT	dup(T)₄	dup(T)₅	dup(T)₆	dup(T)₇	dup(T)₈	dup(T)₉	ins(T)₉C(T)₁₉	dup(T)₁₀	dup(T)₁₁	dup(T)₁₂	dup(T)₁₃	dup(T)₁₅	dup(T)₁₆	ins(T)₁₇	ins(T)₁₈	ins(T)₁₉	ins(T)₂₀	ins(T)₂₁	ins(T)₂₂	ins(T)₂₃	ins(T)₂₄	ins(T)₂₅	ins(T)₂₆	ins(T)₂₇	ins(T)₂₈	ins(T)₂₉	ins(T)₃₀	ins(T)₃₂	ins(T)₃₆
GRCh38.p14 chr 4	NC_000004.12:g.57103661_57103676=	NC_000004.12:g.57103669_57103676del	NC_000004.12:g.57103671_57103676del	NC_000004.12:g.57103672_57103676del	NC_000004.12:g.57103673_57103676del	NC_000004.12:g.57103674_57103676del	NC_000004.12:g.57103675_57103676del	NC_000004.12:g.57103676del	NC_000004.12:g.57103676dup	NC_000004.12:g.57103675_57103676dup	NC_000004.12:g.57103674_57103676dup	NC_000004.12:g.57103673_57103676dup	NC_000004.12:g.57103672_57103676dup	NC_000004.12:g.57103671_57103676dup	NC_000004.12:g.57103670_57103676dup	NC_000004.12:g.57103669_57103676dup	NC_000004.12:g.57103668_57103676dup	NC_000004.12:g.57103661_57103676T[25]CTTTTTTTTTTTTTTTTTTT[1]	NC_000004.12:g.57103667_57103676dup	NC_000004.12:g.57103666_57103676dup	NC_000004.12:g.57103665_57103676dup	NC_000004.12:g.57103664_57103676dup	NC_000004.12:g.57103662_57103676dup	NC_000004.12:g.57103661_57103676dup	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:g.57103676_57103677insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
GRCh37.p13 chr 4	NC_000004.11:g.57969827_57969842=	NC_000004.11:g.57969835_57969842del	NC_000004.11:g.57969837_57969842del	NC_000004.11:g.57969838_57969842del	NC_000004.11:g.57969839_57969842del	NC_000004.11:g.57969840_57969842del	NC_000004.11:g.57969841_57969842del	NC_000004.11:g.57969842del	NC_000004.11:g.57969842dup	NC_000004.11:g.57969841_57969842dup	NC_000004.11:g.57969840_57969842dup	NC_000004.11:g.57969839_57969842dup	NC_000004.11:g.57969838_57969842dup	NC_000004.11:g.57969837_57969842dup	NC_000004.11:g.57969836_57969842dup	NC_000004.11:g.57969835_57969842dup	NC_000004.11:g.57969834_57969842dup	NC_000004.11:g.57969827_57969842T[25]CTTTTTTTTTTTTTTTTTTT[1]	NC_000004.11:g.57969833_57969842dup	NC_000004.11:g.57969832_57969842dup	NC_000004.11:g.57969831_57969842dup	NC_000004.11:g.57969830_57969842dup	NC_000004.11:g.57969828_57969842dup	NC_000004.11:g.57969827_57969842dup	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.11:g.57969842_57969843insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
IGFBP7 RefSeqGene	NG_031877.1:g.11710_11725=	NG_031877.1:g.11718_11725del	NG_031877.1:g.11720_11725del	NG_031877.1:g.11721_11725del	NG_031877.1:g.11722_11725del	NG_031877.1:g.11723_11725del	NG_031877.1:g.11724_11725del	NG_031877.1:g.11725del	NG_031877.1:g.11725dup	NG_031877.1:g.11724_11725dup	NG_031877.1:g.11723_11725dup	NG_031877.1:g.11722_11725dup	NG_031877.1:g.11721_11725dup	NG_031877.1:g.11720_11725dup	NG_031877.1:g.11719_11725dup	NG_031877.1:g.11718_11725dup	NG_031877.1:g.11717_11725dup	NG_031877.1:g.11710_11725A[19]GAAAAAAAAAAAAAAAAAAAAAAAAA[1]	NG_031877.1:g.11716_11725dup	NG_031877.1:g.11715_11725dup	NG_031877.1:g.11714_11725dup	NG_031877.1:g.11713_11725dup	NG_031877.1:g.11711_11725dup	NG_031877.1:g.11710_11725dup	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NG_031877.1:g.11725_11726insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 transcript variant 2	NM_001253835.1:c.475+6216=	NM_001253835.1:c.475+6209_475+6216del	NM_001253835.1:c.475+6211_475+6216del	NM_001253835.1:c.475+6212_475+6216del	NM_001253835.1:c.475+6213_475+6216del	NM_001253835.1:c.475+6214_475+6216del	NM_001253835.1:c.475+6215_475+6216del	NM_001253835.1:c.475+6216del	NM_001253835.1:c.475+6216dup	NM_001253835.1:c.475+6215_475+6216dup	NM_001253835.1:c.475+6214_475+6216dup	NM_001253835.1:c.475+6213_475+6216dup	NM_001253835.1:c.475+6212_475+6216dup	NM_001253835.1:c.475+6211_475+6216dup	NM_001253835.1:c.475+6210_475+6216dup	NM_001253835.1:c.475+6209_475+6216dup	NM_001253835.1:c.475+6208_475+6216dup	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAGAAAAAAAAA	NM_001253835.1:c.475+6207_475+6216dup	NM_001253835.1:c.475+6206_475+6216dup	NM_001253835.1:c.475+6205_475+6216dup	NM_001253835.1:c.475+6204_475+6216dup	NM_001253835.1:c.475+6202_475+6216dup	NM_001253835.1:c.475+6201_475+6216dup	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.1:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 transcript variant 2	NM_001253835.2:c.475+6216=	NM_001253835.2:c.475+6209_475+6216del	NM_001253835.2:c.475+6211_475+6216del	NM_001253835.2:c.475+6212_475+6216del	NM_001253835.2:c.475+6213_475+6216del	NM_001253835.2:c.475+6214_475+6216del	NM_001253835.2:c.475+6215_475+6216del	NM_001253835.2:c.475+6216del	NM_001253835.2:c.475+6216dup	NM_001253835.2:c.475+6215_475+6216dup	NM_001253835.2:c.475+6214_475+6216dup	NM_001253835.2:c.475+6213_475+6216dup	NM_001253835.2:c.475+6212_475+6216dup	NM_001253835.2:c.475+6211_475+6216dup	NM_001253835.2:c.475+6210_475+6216dup	NM_001253835.2:c.475+6209_475+6216dup	NM_001253835.2:c.475+6208_475+6216dup	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAGAAAAAAAAA	NM_001253835.2:c.475+6207_475+6216dup	NM_001253835.2:c.475+6206_475+6216dup	NM_001253835.2:c.475+6205_475+6216dup	NM_001253835.2:c.475+6204_475+6216dup	NM_001253835.2:c.475+6202_475+6216dup	NM_001253835.2:c.475+6201_475+6216dup	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001253835.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 transcript variant 1	NM_001553.2:c.475+6216=	NM_001553.2:c.475+6209_475+6216del	NM_001553.2:c.475+6211_475+6216del	NM_001553.2:c.475+6212_475+6216del	NM_001553.2:c.475+6213_475+6216del	NM_001553.2:c.475+6214_475+6216del	NM_001553.2:c.475+6215_475+6216del	NM_001553.2:c.475+6216del	NM_001553.2:c.475+6216dup	NM_001553.2:c.475+6215_475+6216dup	NM_001553.2:c.475+6214_475+6216dup	NM_001553.2:c.475+6213_475+6216dup	NM_001553.2:c.475+6212_475+6216dup	NM_001553.2:c.475+6211_475+6216dup	NM_001553.2:c.475+6210_475+6216dup	NM_001553.2:c.475+6209_475+6216dup	NM_001553.2:c.475+6208_475+6216dup	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAGAAAAAAAAA	NM_001553.2:c.475+6207_475+6216dup	NM_001553.2:c.475+6206_475+6216dup	NM_001553.2:c.475+6205_475+6216dup	NM_001553.2:c.475+6204_475+6216dup	NM_001553.2:c.475+6202_475+6216dup	NM_001553.2:c.475+6201_475+6216dup	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.2:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
IGFBP7 transcript variant 1	NM_001553.3:c.475+6216=	NM_001553.3:c.475+6209_475+6216del	NM_001553.3:c.475+6211_475+6216del	NM_001553.3:c.475+6212_475+6216del	NM_001553.3:c.475+6213_475+6216del	NM_001553.3:c.475+6214_475+6216del	NM_001553.3:c.475+6215_475+6216del	NM_001553.3:c.475+6216del	NM_001553.3:c.475+6216dup	NM_001553.3:c.475+6215_475+6216dup	NM_001553.3:c.475+6214_475+6216dup	NM_001553.3:c.475+6213_475+6216dup	NM_001553.3:c.475+6212_475+6216dup	NM_001553.3:c.475+6211_475+6216dup	NM_001553.3:c.475+6210_475+6216dup	NM_001553.3:c.475+6209_475+6216dup	NM_001553.3:c.475+6208_475+6216dup	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAGAAAAAAAAA	NM_001553.3:c.475+6207_475+6216dup	NM_001553.3:c.475+6206_475+6216dup	NM_001553.3:c.475+6205_475+6216dup	NM_001553.3:c.475+6204_475+6216dup	NM_001553.3:c.475+6202_475+6216dup	NM_001553.3:c.475+6201_475+6216dup	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NM_001553.3:c.475+6216_475+6217insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

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#.

74 SubSNP, 47 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	HGSV	ss80018620	Dec 15, 2007 (129)
2	HUMANGENOME_JCVI	ss95355211	Feb 05, 2009 (130)
3	PJP	ss295166207	May 09, 2011 (137)
4	PJP	ss295166208	May 09, 2011 (137)
5	DDI	ss1536407753	Apr 01, 2015 (144)
6	SWEGEN	ss2994706344	Nov 08, 2017 (151)
7	SWEGEN	ss2994706345	Nov 08, 2017 (151)
8	SWEGEN	ss2994706346	Nov 08, 2017 (151)
9	SWEGEN	ss2994706347	Nov 08, 2017 (151)
10	URBANLAB	ss3647730370	Oct 12, 2018 (152)
11	EVA_DECODE	ss3712060469	Jul 13, 2019 (153)
12	EVA_DECODE	ss3712060470	Jul 13, 2019 (153)
13	EVA_DECODE	ss3712060471	Jul 13, 2019 (153)
14	EVA_DECODE	ss3712060472	Jul 13, 2019 (153)
15	EVA_DECODE	ss3712060473	Jul 13, 2019 (153)
16	PACBIO	ss3784714513	Jul 13, 2019 (153)
17	PACBIO	ss3790171898	Jul 13, 2019 (153)
18	PACBIO	ss3795046984	Jul 13, 2019 (153)
19	EVA	ss3828542035	Apr 26, 2020 (154)
20	GNOMAD	ss4111356891	Apr 26, 2021 (155)
21	GNOMAD	ss4111356892	Apr 26, 2021 (155)
22	GNOMAD	ss4111356893	Apr 26, 2021 (155)
23	GNOMAD	ss4111356895	Apr 26, 2021 (155)
24	GNOMAD	ss4111356896	Apr 26, 2021 (155)
25	GNOMAD	ss4111356897	Apr 26, 2021 (155)
26	GNOMAD	ss4111356899	Apr 26, 2021 (155)
27	GNOMAD	ss4111356900	Apr 26, 2021 (155)
28	GNOMAD	ss4111356901	Apr 26, 2021 (155)
29	GNOMAD	ss4111356902	Apr 26, 2021 (155)
30	GNOMAD	ss4111356903	Apr 26, 2021 (155)
31	GNOMAD	ss4111356904	Apr 26, 2021 (155)
32	GNOMAD	ss4111356905	Apr 26, 2021 (155)
33	GNOMAD	ss4111356906	Apr 26, 2021 (155)
34	GNOMAD	ss4111356907	Apr 26, 2021 (155)
35	GNOMAD	ss4111356908	Apr 26, 2021 (155)
36	GNOMAD	ss4111356909	Apr 26, 2021 (155)
37	GNOMAD	ss4111356910	Apr 26, 2021 (155)
38	GNOMAD	ss4111356911	Apr 26, 2021 (155)
39	GNOMAD	ss4111356912	Apr 26, 2021 (155)
40	GNOMAD	ss4111356913	Apr 26, 2021 (155)
41	GNOMAD	ss4111356914	Apr 26, 2021 (155)
42	GNOMAD	ss4111356915	Apr 26, 2021 (155)
43	GNOMAD	ss4111356916	Apr 26, 2021 (155)
44	GNOMAD	ss4111356917	Apr 26, 2021 (155)
45	GNOMAD	ss4111356918	Apr 26, 2021 (155)
46	GNOMAD	ss4111356919	Apr 26, 2021 (155)
47	GNOMAD	ss4111356920	Apr 26, 2021 (155)
48	GNOMAD	ss4111356921	Apr 26, 2021 (155)
49	GNOMAD	ss4111356922	Apr 26, 2021 (155)
50	GNOMAD	ss4111356923	Apr 26, 2021 (155)
51	GNOMAD	ss4111356924	Apr 26, 2021 (155)
52	GNOMAD	ss4111356925	Apr 26, 2021 (155)
53	GNOMAD	ss4111356926	Apr 26, 2021 (155)
54	GNOMAD	ss4111356927	Apr 26, 2021 (155)
55	GNOMAD	ss4111356928	Apr 26, 2021 (155)
56	TOMMO_GENOMICS	ss5165732563	Apr 26, 2021 (155)
57	TOMMO_GENOMICS	ss5165732564	Apr 26, 2021 (155)
58	TOMMO_GENOMICS	ss5165732565	Apr 26, 2021 (155)
59	TOMMO_GENOMICS	ss5165732566	Apr 26, 2021 (155)
60	TOMMO_GENOMICS	ss5165732567	Apr 26, 2021 (155)
61	1000G_HIGH_COVERAGE	ss5259213568	Oct 13, 2022 (156)
62	1000G_HIGH_COVERAGE	ss5259213569	Oct 13, 2022 (156)
63	1000G_HIGH_COVERAGE	ss5259213570	Oct 13, 2022 (156)
64	HUGCELL_USP	ss5457972998	Oct 13, 2022 (156)
65	HUGCELL_USP	ss5457973000	Oct 13, 2022 (156)
66	HUGCELL_USP	ss5457973001	Oct 13, 2022 (156)
67	TOMMO_GENOMICS	ss5700082392	Oct 13, 2022 (156)
68	TOMMO_GENOMICS	ss5700082393	Oct 13, 2022 (156)
69	TOMMO_GENOMICS	ss5700082395	Oct 13, 2022 (156)
70	TOMMO_GENOMICS	ss5700082396	Oct 13, 2022 (156)
71	TOMMO_GENOMICS	ss5700082397	Oct 13, 2022 (156)
72	EVA	ss5844002119	Oct 13, 2022 (156)
73	EVA	ss5844002120	Oct 13, 2022 (156)
74	EVA	ss5844002121	Oct 13, 2022 (156)
75	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
76	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
77	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
78	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
79	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
80	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
81	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
82	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
83	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
84	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
85	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
86	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
87	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
88	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
89	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
90	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
91	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
92	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
93	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
94	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
95	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
96	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
97	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
98	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
99	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
100	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
101	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
102	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
103	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
104	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
105	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
106	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
107	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
108	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
109	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
110	gnomAD - Genomes Submission ignored due to conflicting rows: Row 149862868 (NC_000004.12:57103660::T 15/81544) Row 149862869 (NC_000004.12:57103660::TT 50/81546) Row 149862870 (NC_000004.12:57103660::TTT 22346/80898)...	-	Apr 26, 2021 (155)
111	8.3KJPN Submission ignored due to conflicting rows: Row 23701870 (NC_000004.11:57969826::TTT 6424/14928) Row 23701871 (NC_000004.11:57969826::TTTT 3998/14928) Row 23701872 (NC_000004.11:57969826::TTTTTTTTT 64/14928)...	-	Apr 26, 2021 (155)
112	8.3KJPN Submission ignored due to conflicting rows: Row 23701870 (NC_000004.11:57969826::TTT 6424/14928) Row 23701871 (NC_000004.11:57969826::TTTT 3998/14928) Row 23701872 (NC_000004.11:57969826::TTTTTTTTT 64/14928)...	-	Apr 26, 2021 (155)
113	8.3KJPN Submission ignored due to conflicting rows: Row 23701870 (NC_000004.11:57969826::TTT 6424/14928) Row 23701871 (NC_000004.11:57969826::TTTT 3998/14928) Row 23701872 (NC_000004.11:57969826::TTTTTTTTT 64/14928)...	-	Apr 26, 2021 (155)
114	8.3KJPN Submission ignored due to conflicting rows: Row 23701870 (NC_000004.11:57969826::TTT 6424/14928) Row 23701871 (NC_000004.11:57969826::TTTT 3998/14928) Row 23701872 (NC_000004.11:57969826::TTTTTTTTT 64/14928)...	-	Apr 26, 2021 (155)
115	8.3KJPN Submission ignored due to conflicting rows: Row 23701870 (NC_000004.11:57969826::TTT 6424/14928) Row 23701871 (NC_000004.11:57969826::TTTT 3998/14928) Row 23701872 (NC_000004.11:57969826::TTTTTTTTT 64/14928)...	-	Apr 26, 2021 (155)
116	14KJPN Submission ignored due to conflicting rows: Row 33919496 (NC_000004.12:57103660::TTT 12706/26694) Row 33919497 (NC_000004.12:57103660::TTTT 7827/26694) Row 33919499 (NC_000004.12:57103660::TTTTT 644/26694)...	-	Oct 13, 2022 (156)
117	14KJPN Submission ignored due to conflicting rows: Row 33919496 (NC_000004.12:57103660::TTT 12706/26694) Row 33919497 (NC_000004.12:57103660::TTTT 7827/26694) Row 33919499 (NC_000004.12:57103660::TTTTT 644/26694)...	-	Oct 13, 2022 (156)
118	14KJPN Submission ignored due to conflicting rows: Row 33919496 (NC_000004.12:57103660::TTT 12706/26694) Row 33919497 (NC_000004.12:57103660::TTTT 7827/26694) Row 33919499 (NC_000004.12:57103660::TTTTT 644/26694)...	-	Oct 13, 2022 (156)
119	14KJPN Submission ignored due to conflicting rows: Row 33919496 (NC_000004.12:57103660::TTT 12706/26694) Row 33919497 (NC_000004.12:57103660::TTTT 7827/26694) Row 33919499 (NC_000004.12:57103660::TTTTT 644/26694)...	-	Oct 13, 2022 (156)
120	14KJPN Submission ignored due to conflicting rows: Row 33919496 (NC_000004.12:57103660::TTT 12706/26694) Row 33919497 (NC_000004.12:57103660::TTTT 7827/26694) Row 33919499 (NC_000004.12:57103660::TTTTT 644/26694)...	-	Oct 13, 2022 (156)
121	ALFA	NC_000004.12 - 57103661	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)
rs142272920	May 11, 2012 (137)
rs148728966	May 11, 2012 (137)

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTT	(self)
ss4111356928	NC_000004.12:57103660:TTTTTT:	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTT	(self)
ss4111356927	NC_000004.12:57103660:TTTT:	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT	(self)
ss4111356926	NC_000004.12:57103660:TT:	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT	(self)
ss4111356925	NC_000004.12:57103660:T:	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT	(self)
ss4111356891	NC_000004.12:57103660::T	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT	(self)
ss5165732566	NC_000004.11:57969826::TT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss3712060469, ss4111356892, ss5259213570, ss5700082396	NC_000004.12:57103660::TT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT	(self)
ss2994706346, ss3828542035, ss5165732563, ss5844002121	NC_000004.11:57969826::TTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss3712060470, ss4111356893, ss5457972998, ss5700082392	NC_000004.12:57103660::TTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT	(self)
ss295166207	NC_000004.10:57664584::TTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss295166208	NC_000004.10:57664596::TTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss1536407753, ss2994706344, ss3784714513, ss3790171898, ss3795046984, ss5165732564, ss5844002120	NC_000004.11:57969826::TTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss3647730370, ss3712060471, ss4111356895, ss5457973000, ss5700082393	NC_000004.12:57103660::TTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss80018620, ss95355211	NT_022853.15:5309725::TTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT	(self)
ss2994706345, ss5165732567, ss5844002119	NC_000004.11:57969826::TTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss3712060472, ss4111356896, ss5259213568, ss5457973001, ss5700082395	NC_000004.12:57103660::TTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT	(self)
ss2994706347	NC_000004.11:57969826::TTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss3712060473, ss4111356897, ss5259213569	NC_000004.12:57103660::TTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356899	NC_000004.12:57103660::TTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
9384192765	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356900	NC_000004.12:57103660::TTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss5165732565	NC_000004.11:57969826::TTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356901, ss5700082397	NC_000004.12:57103660::TTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356917	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTCTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTT	(self)
ss4111356902	NC_000004.12:57103660::TTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356903	NC_000004.12:57103660::TTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356904	NC_000004.12:57103660::TTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356905	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356906	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356907	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356908	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356909	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356910	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356911	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356912	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356913	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356914	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356915	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356916	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356918	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356919	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356920	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356921	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356922	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356923	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)
ss4111356924	NC_000004.12:57103660::TTTTTTTTTTT… NC_000004.12:57103660::TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Destination RSIDs
ss3429167090	NC_000004.12:57103660:TTTTT:	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTTTTT
ss3429167092	NC_000004.12:57103660:TTTTTTTT:	NC_000004.12:57103660:TTTTTTTTTTTT… NC_000004.12:57103660:TTTTTTTTTTTTTTTT:TTTTTTTT

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

No publications for rs59173874

The Flanks tab provides retrieving flanking sequences of a SNP on all molecules that have placements.

Genome context:

Select flank length:

Genomic regions, transcripts, and products
Top▲ Help
NCBI Graphical Sequence Viewer display of the genomic region, transcripts and protein products for the reported RefSNP (rs).
Use the zoom option to view the nucleotides around the RefSNP and find other neighboring RefSNPs.
Visit Sequence Viewer for help with navigating inside the display and modifying the selection of displayed data tracks.

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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs59173874