Name: rs1491543645
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.

rs1491543645

Current Build 156

Released September 21, 2022

Organism: Homo sapiens
Position: chr10:121524100 (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: insCA / insCACA / ins(CA)₃ / ins(C…
insCA / insCACA / ins(CA)₃ / ins(CA)₄ / ins(CA)₅ / ins(CA)₆ / ins(CA)₇ / insCATACA / insCATACACA / insCAT(AC)₃A / insCAT(AC)₄A / insCAT(AC)₅A
Variation Type: Indel Insertion and Deletion
Frequency: insCA=0.00000 (0/12064, ALFA)
insCACA=0.00000 (0/12064, ALFA)
ins(CA)₃=0.00000 (0/12064, ALFA) (+ 9 more)
ins(CA)₄=0.00000 (0/12064, ALFA)
ins(CA)₅=0.00000 (0/12064, ALFA)
ins(CA)₆=0.00000 (0/12064, ALFA)
ins(CA)₇=0.00000 (0/12064, ALFA)
insCATACA=0.00000 (0/12064, ALFA)
insCATACACA=0.00000 (0/12064, ALFA)
insCAT(AC)₃A=0.00000 (0/12064, ALFA)
insCAT(AC)₄A=0.00000 (0/12064, ALFA)
insCAT(AC)₅A=0.00000 (0/12064, ALFA)

Clinical Significance: Not Reported in ClinVar
Gene : Consequence: FGFR2 : 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	12024	A=1.00000	ACA=0.00000, ACACA=0.00000, ACACACA=0.00000, ACACACACA=0.00000, ACACACACACA=0.00000, ACACACACACACA=0.00000, ACACACACACACACA=0.00000, ACATACA=0.00000, ACATACACA=0.00000, ACATACACACA=0.00000, ACATACACACACA=0.00000, ACATACACACACACA=0.00000	1.0	N/A
European	Sub	7608	A=1.0000	ACA=0.0000, ACACA=0.0000, ACACACA=0.0000, ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACATACA=0.0000, ACATACACA=0.0000, ACATACACACA=0.0000, ACATACACACACA=0.0000, ACATACACACACACA=0.0000	1.0	N/A
African	Sub	2970	A=1.0000	ACA=0.0000, ACACA=0.0000, ACACACA=0.0000, ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACATACA=0.0000, ACATACACA=0.0000, ACATACACACA=0.0000, ACATACACACACA=0.0000, ACATACACACACACA=0.0000	1.0	N/A
African Others	Sub	98	A=1.00	ACA=0.00, ACACA=0.00, ACACACA=0.00, ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACATACA=0.00, ACATACACA=0.00, ACATACACACA=0.00, ACATACACACACA=0.00, ACATACACACACACA=0.00	1.0	N/A
African American	Sub	2872	A=1.0000	ACA=0.0000, ACACA=0.0000, ACACACA=0.0000, ACACACACA=0.0000, ACACACACACA=0.0000, ACACACACACACA=0.0000, ACACACACACACACA=0.0000, ACATACA=0.0000, ACATACACA=0.0000, ACATACACACA=0.0000, ACATACACACACA=0.0000, ACATACACACACACA=0.0000	1.0	N/A
Asian	Sub	126	A=1.000	ACA=0.000, ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACATACA=0.000, ACATACACA=0.000, ACATACACACA=0.000, ACATACACACACA=0.000, ACATACACACACACA=0.000	1.0	N/A
East Asian	Sub	104	A=1.000	ACA=0.000, ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACATACA=0.000, ACATACACA=0.000, ACATACACACA=0.000, ACATACACACACA=0.000, ACATACACACACACA=0.000	1.0	N/A
Other Asian	Sub	22	A=1.00	ACA=0.00, ACACA=0.00, ACACACA=0.00, ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACATACA=0.00, ACATACACA=0.00, ACATACACACA=0.00, ACATACACACACA=0.00, ACATACACACACACA=0.00	1.0	N/A
Latin American 1	Sub	142	A=1.000	ACA=0.000, ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACATACA=0.000, ACATACACA=0.000, ACATACACACA=0.000, ACATACACACACA=0.000, ACATACACACACACA=0.000	1.0	N/A
Latin American 2	Sub	532	A=1.000	ACA=0.000, ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACATACA=0.000, ACATACACA=0.000, ACATACACACA=0.000, ACATACACACACA=0.000, ACATACACACACACA=0.000	1.0	N/A
South Asian	Sub	96	A=1.00	ACA=0.00, ACACA=0.00, ACACACA=0.00, ACACACACA=0.00, ACACACACACA=0.00, ACACACACACACA=0.00, ACACACACACACACA=0.00, ACATACA=0.00, ACATACACA=0.00, ACATACACACA=0.00, ACATACACACACA=0.00, ACATACACACACACA=0.00	1.0	N/A
Other	Sub	550	A=1.000	ACA=0.000, ACACA=0.000, ACACACA=0.000, ACACACACA=0.000, ACACACACACA=0.000, ACACACACACACA=0.000, ACACACACACACACA=0.000, ACATACA=0.000, ACATACACA=0.000, ACATACACACA=0.000, ACATACACACACA=0.000, ACATACACACACACA=0.000	1.0	N/A

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

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Study	Population	Group	Sample Size	Ref Allele	Alt Allele
Allele Frequency Aggregator	Total	Global	12064	A=0.99834	insCA=0.00000, insCACA=0.00000, ins(CA)₃=0.00000, ins(CA)₄=0.00000, ins(CA)₅=0.00000, ins(CA)₆=0.00000, ins(CA)₇=0.00000, insCATACA=0.00000, insCATACACA=0.00000, insCAT(AC)₃A=0.00000, insCAT(AC)₄A=0.00000, insCAT(AC)₅A=0.00000
Allele Frequency Aggregator	European	Sub	7608	A=1.0000	insCA=0.0000, insCACA=0.0000, ins(CA)₃=0.0000, ins(CA)₄=0.0000, ins(CA)₅=0.0000, ins(CA)₆=0.0000, ins(CA)₇=0.0000, insCATACA=0.0000, insCATACACA=0.0000, insCAT(AC)₃A=0.0000, insCAT(AC)₄A=0.0000, insCAT(AC)₅A=0.0000
Allele Frequency Aggregator	African	Sub	2996	A=0.9957	insCA=0.0000, insCACA=0.0000, ins(CA)₃=0.0000, ins(CA)₄=0.0000, ins(CA)₅=0.0000, ins(CA)₆=0.0000, ins(CA)₇=0.0000, insCATACA=0.0000, insCATACACA=0.0000, insCAT(AC)₃A=0.0000, insCAT(AC)₄A=0.0000, insCAT(AC)₅A=0.0000
Allele Frequency Aggregator	Other	Sub	558	A=0.993	insCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, insCATACA=0.000, insCATACACA=0.000, insCAT(AC)₃A=0.000, insCAT(AC)₄A=0.000, insCAT(AC)₅A=0.000
Allele Frequency Aggregator	Latin American 2	Sub	532	A=1.000	insCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, insCATACA=0.000, insCATACACA=0.000, insCAT(AC)₃A=0.000, insCAT(AC)₄A=0.000, insCAT(AC)₅A=0.000
Allele Frequency Aggregator	Latin American 1	Sub	142	A=1.000	insCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, insCATACA=0.000, insCATACACA=0.000, insCAT(AC)₃A=0.000, insCAT(AC)₄A=0.000, insCAT(AC)₅A=0.000
Allele Frequency Aggregator	Asian	Sub	132	A=0.977	insCA=0.000, insCACA=0.000, ins(CA)₃=0.000, ins(CA)₄=0.000, ins(CA)₅=0.000, ins(CA)₆=0.000, ins(CA)₇=0.000, insCATACA=0.000, insCATACACA=0.000, insCAT(AC)₃A=0.000, insCAT(AC)₄A=0.000, insCAT(AC)₅A=0.000
Allele Frequency Aggregator	South Asian	Sub	96	A=1.00	insCA=0.00, insCACA=0.00, ins(CA)₃=0.00, ins(CA)₄=0.00, ins(CA)₅=0.00, ins(CA)₆=0.00, ins(CA)₇=0.00, insCATACA=0.00, insCATACACA=0.00, insCAT(AC)₃A=0.00, insCAT(AC)₄A=0.00, insCAT(AC)₅A=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 10	NC_000010.11:g.121524100_121524101insCA
GRCh38.p14 chr 10	NC_000010.11:g.121524100_121524101insCACA
GRCh38.p14 chr 10	NC_000010.11:g.121524101CA[3]
GRCh38.p14 chr 10	NC_000010.11:g.121524101CA[4]
GRCh38.p14 chr 10	NC_000010.11:g.121524101CA[5]
GRCh38.p14 chr 10	NC_000010.11:g.121524101CA[6]
GRCh38.p14 chr 10	NC_000010.11:g.121524101CA[7]
GRCh38.p14 chr 10	NC_000010.11:g.121524100_121524101insCATACA
GRCh38.p14 chr 10	NC_000010.11:g.121524100_121524101insCATACACA
GRCh38.p14 chr 10	NC_000010.11:g.121524100_121524101insCATACACACA
GRCh38.p14 chr 10	NC_000010.11:g.121524100_121524101insCATACACACACA
GRCh38.p14 chr 10	NC_000010.11:g.121524100_121524101insCATACACACACACA
GRCh37.p13 chr 10	NC_000010.10:g.123283614_123283615insCA
GRCh37.p13 chr 10	NC_000010.10:g.123283614_123283615insCACA
GRCh37.p13 chr 10	NC_000010.10:g.123283615CA[3]
GRCh37.p13 chr 10	NC_000010.10:g.123283615CA[4]
GRCh37.p13 chr 10	NC_000010.10:g.123283615CA[5]
GRCh37.p13 chr 10	NC_000010.10:g.123283615CA[6]
GRCh37.p13 chr 10	NC_000010.10:g.123283615CA[7]
GRCh37.p13 chr 10	NC_000010.10:g.123283614_123283615insCATACA
GRCh37.p13 chr 10	NC_000010.10:g.123283614_123283615insCATACACA
GRCh37.p13 chr 10	NC_000010.10:g.123283614_123283615insCATACACACA
GRCh37.p13 chr 10	NC_000010.10:g.123283614_123283615insCATACACACACA
GRCh37.p13 chr 10	NC_000010.10:g.123283614_123283615insCATACACACACACA
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359_79360insGT
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359_79360insGTGT
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79360GT[3]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79360GT[4]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79360GT[5]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79360GT[6]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79360GT[7]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359_79360insGTATGT
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359TG[2]TATGT[1]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359TG[3]TATGT[1]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359TG[4]TATGT[1]
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359TG[5]TATGT[1]

Gene: FGFR2, fibroblast growth factor receptor 2 (minus strand)

Molecule type	Change	Amino acid[Codon]	SO Term
FGFR2 transcript variant 1	NM_000141.5:c.749-3931_74… NM_000141.5:c.749-3931_749-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 3	NM_001144913.1:c.749-3931… NM_001144913.1:c.749-3931_749-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 4	NM_001144914.1:c.749-8781… NM_001144914.1:c.749-8781_749-8780insTG	N/A	Intron Variant
FGFR2 transcript variant 5	NM_001144915.2:c.482-3931… NM_001144915.2:c.482-3931_482-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 6	NM_001144916.2:c.404-3931… NM_001144916.2:c.404-3931_404-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 7	NM_001144917.2:c.749-3931… NM_001144917.2:c.749-3931_749-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 8	NM_001144918.2:c.404-3931… NM_001144918.2:c.404-3931_404-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 9	NM_001144919.2:c.482-3931… NM_001144919.2:c.482-3931_482-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 15	NM_001320654.2:c.64+2055_… NM_001320654.2:c.64+2055_64+2056insTG	N/A	Intron Variant
FGFR2 transcript variant 16	NM_001320658.2:c.749-3931… NM_001320658.2:c.749-3931_749-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 2	NM_022970.3:c.749-3931_74… NM_022970.3:c.749-3931_749-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 11	NM_023029.2:c.482-3931_48… NM_023029.2:c.482-3931_482-3930insTG	N/A	Intron Variant
FGFR2 transcript variant 14	NR_073009.2:n.	N/A	Intron Variant
FGFR2 transcript variant X1	XM_006717708.4:c.806-3931… XM_006717708.4:c.806-3931_806-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X2	XM_006717710.5:c.806-3931… XM_006717710.5:c.806-3931_806-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X3	XM_017015920.3:c.806-3931… XM_017015920.3:c.806-3931_806-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X4	XM_017015921.3:c.806-3931… XM_017015921.3:c.806-3931_806-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X10	XM_017015924.3:c.461-3931… XM_017015924.3:c.461-3931_461-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X11	XM_017015925.3:c.461-3931… XM_017015925.3:c.461-3931_461-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X6	XM_024447887.2:c.539-3931… XM_024447887.2:c.539-3931_539-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X7	XM_024447888.2:c.539-3931… XM_024447888.2:c.539-3931_539-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X8	XM_024447889.2:c.539-3931… XM_024447889.2:c.539-3931_539-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X5	XM_024447890.2:c.539-3931… XM_024447890.2:c.539-3931_539-3930insTG	N/A	Intron Variant
FGFR2 transcript variant X9	XM_024447891.2:c.461-3931… XM_024447891.2:c.461-3931_461-3930insTG	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=	insCA	insCACA	ins(CA)₃	ins(CA)₄	ins(CA)₅	ins(CA)₆	ins(CA)₇	insCATACA	insCATACACA	insCAT(AC)₃A	insCAT(AC)₄A	insCAT(AC)₅A
GRCh38.p14 chr 10	NC_000010.11:g.121524100=	NC_000010.11:g.121524100_121524101insCA	NC_000010.11:g.121524100_121524101insCACA	NC_000010.11:g.121524101CA[3]	NC_000010.11:g.121524101CA[4]	NC_000010.11:g.121524101CA[5]	NC_000010.11:g.121524101CA[6]	NC_000010.11:g.121524101CA[7]	NC_000010.11:g.121524100_121524101insCATACA	NC_000010.11:g.121524100_121524101insCATACACA	NC_000010.11:g.121524100_121524101insCATACACACA	NC_000010.11:g.121524100_121524101insCATACACACACA	NC_000010.11:g.121524100_121524101insCATACACACACACA
GRCh37.p13 chr 10	NC_000010.10:g.123283614=	NC_000010.10:g.123283614_123283615insCA	NC_000010.10:g.123283614_123283615insCACA	NC_000010.10:g.123283615CA[3]	NC_000010.10:g.123283615CA[4]	NC_000010.10:g.123283615CA[5]	NC_000010.10:g.123283615CA[6]	NC_000010.10:g.123283615CA[7]	NC_000010.10:g.123283614_123283615insCATACA	NC_000010.10:g.123283614_123283615insCATACACA	NC_000010.10:g.123283614_123283615insCATACACACA	NC_000010.10:g.123283614_123283615insCATACACACACA	NC_000010.10:g.123283614_123283615insCATACACACACACA
FGFR2 RefSeqGene (LRG_994)	NG_012449.2:g.79359=	NG_012449.2:g.79359_79360insGT	NG_012449.2:g.79359_79360insGTGT	NG_012449.2:g.79360GT[3]	NG_012449.2:g.79360GT[4]	NG_012449.2:g.79360GT[5]	NG_012449.2:g.79360GT[6]	NG_012449.2:g.79360GT[7]	NG_012449.2:g.79359_79360insGTATGT	NG_012449.2:g.79359TG[2]TATGT[1]	NG_012449.2:g.79359TG[3]TATGT[1]	NG_012449.2:g.79359TG[4]TATGT[1]	NG_012449.2:g.79359TG[5]TATGT[1]
FGFR2 transcript variant 1	NM_000141.4:c.749-3931=	NM_000141.4:c.749-3931_749-3930insTG	NM_000141.4:c.749-3931_749-3930insTGTG	NM_000141.4:c.749-3931_749-3930insTGTGTG	NM_000141.4:c.749-3931_749-3930insTGTGTGTG	NM_000141.4:c.749-3931_749-3930insTGTGTGTGTG	NM_000141.4:c.749-3931_749-3930insTGTGTGTGTGTG	NM_000141.4:c.749-3931_749-3930insTGTGTGTGTGTGTG	NM_000141.4:c.749-3931_749-3930insTGTATG	NM_000141.4:c.749-3931_749-3930insTGTGTATG	NM_000141.4:c.749-3931_749-3930insTGTGTGTATG	NM_000141.4:c.749-3931_749-3930insTGTGTGTGTATG	NM_000141.4:c.749-3931_749-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 1	NM_000141.5:c.749-3931=	NM_000141.5:c.749-3931_749-3930insTG	NM_000141.5:c.749-3931_749-3930insTGTG	NM_000141.5:c.749-3931_749-3930insTGTGTG	NM_000141.5:c.749-3931_749-3930insTGTGTGTG	NM_000141.5:c.749-3931_749-3930insTGTGTGTGTG	NM_000141.5:c.749-3931_749-3930insTGTGTGTGTGTG	NM_000141.5:c.749-3931_749-3930insTGTGTGTGTGTGTG	NM_000141.5:c.749-3931_749-3930insTGTATG	NM_000141.5:c.749-3931_749-3930insTGTGTATG	NM_000141.5:c.749-3931_749-3930insTGTGTGTATG	NM_000141.5:c.749-3931_749-3930insTGTGTGTGTATG	NM_000141.5:c.749-3931_749-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 3	NM_001144913.1:c.749-3931=	NM_001144913.1:c.749-3931_749-3930insTG	NM_001144913.1:c.749-3931_749-3930insTGTG	NM_001144913.1:c.749-3931_749-3930insTGTGTG	NM_001144913.1:c.749-3931_749-3930insTGTGTGTG	NM_001144913.1:c.749-3931_749-3930insTGTGTGTGTG	NM_001144913.1:c.749-3931_749-3930insTGTGTGTGTGTG	NM_001144913.1:c.749-3931_749-3930insTGTGTGTGTGTGTG	NM_001144913.1:c.749-3931_749-3930insTGTATG	NM_001144913.1:c.749-3931_749-3930insTGTGTATG	NM_001144913.1:c.749-3931_749-3930insTGTGTGTATG	NM_001144913.1:c.749-3931_749-3930insTGTGTGTGTATG	NM_001144913.1:c.749-3931_749-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 4	NM_001144914.1:c.749-8781=	NM_001144914.1:c.749-8781_749-8780insTG	NM_001144914.1:c.749-8781_749-8780insTGTG	NM_001144914.1:c.749-8781_749-8780insTGTGTG	NM_001144914.1:c.749-8781_749-8780insTGTGTGTG	NM_001144914.1:c.749-8781_749-8780insTGTGTGTGTG	NM_001144914.1:c.749-8781_749-8780insTGTGTGTGTGTG	NM_001144914.1:c.749-8781_749-8780insTGTGTGTGTGTGTG	NM_001144914.1:c.749-8781_749-8780insTGTATG	NM_001144914.1:c.749-8781_749-8780insTGTGTATG	NM_001144914.1:c.749-8781_749-8780insTGTGTGTATG	NM_001144914.1:c.749-8781_749-8780insTGTGTGTGTATG	NM_001144914.1:c.749-8781_749-8780insTGTGTGTGTGTATG
FGFR2 transcript variant 5	NM_001144915.1:c.482-3931=	NM_001144915.1:c.482-3931_482-3930insTG	NM_001144915.1:c.482-3931_482-3930insTGTG	NM_001144915.1:c.482-3931_482-3930insTGTGTG	NM_001144915.1:c.482-3931_482-3930insTGTGTGTG	NM_001144915.1:c.482-3931_482-3930insTGTGTGTGTG	NM_001144915.1:c.482-3931_482-3930insTGTGTGTGTGTG	NM_001144915.1:c.482-3931_482-3930insTGTGTGTGTGTGTG	NM_001144915.1:c.482-3931_482-3930insTGTATG	NM_001144915.1:c.482-3931_482-3930insTGTGTATG	NM_001144915.1:c.482-3931_482-3930insTGTGTGTATG	NM_001144915.1:c.482-3931_482-3930insTGTGTGTGTATG	NM_001144915.1:c.482-3931_482-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 5	NM_001144915.2:c.482-3931=	NM_001144915.2:c.482-3931_482-3930insTG	NM_001144915.2:c.482-3931_482-3930insTGTG	NM_001144915.2:c.482-3931_482-3930insTGTGTG	NM_001144915.2:c.482-3931_482-3930insTGTGTGTG	NM_001144915.2:c.482-3931_482-3930insTGTGTGTGTG	NM_001144915.2:c.482-3931_482-3930insTGTGTGTGTGTG	NM_001144915.2:c.482-3931_482-3930insTGTGTGTGTGTGTG	NM_001144915.2:c.482-3931_482-3930insTGTATG	NM_001144915.2:c.482-3931_482-3930insTGTGTATG	NM_001144915.2:c.482-3931_482-3930insTGTGTGTATG	NM_001144915.2:c.482-3931_482-3930insTGTGTGTGTATG	NM_001144915.2:c.482-3931_482-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 6	NM_001144916.1:c.404-3931=	NM_001144916.1:c.404-3931_404-3930insTG	NM_001144916.1:c.404-3931_404-3930insTGTG	NM_001144916.1:c.404-3931_404-3930insTGTGTG	NM_001144916.1:c.404-3931_404-3930insTGTGTGTG	NM_001144916.1:c.404-3931_404-3930insTGTGTGTGTG	NM_001144916.1:c.404-3931_404-3930insTGTGTGTGTGTG	NM_001144916.1:c.404-3931_404-3930insTGTGTGTGTGTGTG	NM_001144916.1:c.404-3931_404-3930insTGTATG	NM_001144916.1:c.404-3931_404-3930insTGTGTATG	NM_001144916.1:c.404-3931_404-3930insTGTGTGTATG	NM_001144916.1:c.404-3931_404-3930insTGTGTGTGTATG	NM_001144916.1:c.404-3931_404-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 6	NM_001144916.2:c.404-3931=	NM_001144916.2:c.404-3931_404-3930insTG	NM_001144916.2:c.404-3931_404-3930insTGTG	NM_001144916.2:c.404-3931_404-3930insTGTGTG	NM_001144916.2:c.404-3931_404-3930insTGTGTGTG	NM_001144916.2:c.404-3931_404-3930insTGTGTGTGTG	NM_001144916.2:c.404-3931_404-3930insTGTGTGTGTGTG	NM_001144916.2:c.404-3931_404-3930insTGTGTGTGTGTGTG	NM_001144916.2:c.404-3931_404-3930insTGTATG	NM_001144916.2:c.404-3931_404-3930insTGTGTATG	NM_001144916.2:c.404-3931_404-3930insTGTGTGTATG	NM_001144916.2:c.404-3931_404-3930insTGTGTGTGTATG	NM_001144916.2:c.404-3931_404-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 7	NM_001144917.1:c.749-3931=	NM_001144917.1:c.749-3931_749-3930insTG	NM_001144917.1:c.749-3931_749-3930insTGTG	NM_001144917.1:c.749-3931_749-3930insTGTGTG	NM_001144917.1:c.749-3931_749-3930insTGTGTGTG	NM_001144917.1:c.749-3931_749-3930insTGTGTGTGTG	NM_001144917.1:c.749-3931_749-3930insTGTGTGTGTGTG	NM_001144917.1:c.749-3931_749-3930insTGTGTGTGTGTGTG	NM_001144917.1:c.749-3931_749-3930insTGTATG	NM_001144917.1:c.749-3931_749-3930insTGTGTATG	NM_001144917.1:c.749-3931_749-3930insTGTGTGTATG	NM_001144917.1:c.749-3931_749-3930insTGTGTGTGTATG	NM_001144917.1:c.749-3931_749-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 7	NM_001144917.2:c.749-3931=	NM_001144917.2:c.749-3931_749-3930insTG	NM_001144917.2:c.749-3931_749-3930insTGTG	NM_001144917.2:c.749-3931_749-3930insTGTGTG	NM_001144917.2:c.749-3931_749-3930insTGTGTGTG	NM_001144917.2:c.749-3931_749-3930insTGTGTGTGTG	NM_001144917.2:c.749-3931_749-3930insTGTGTGTGTGTG	NM_001144917.2:c.749-3931_749-3930insTGTGTGTGTGTGTG	NM_001144917.2:c.749-3931_749-3930insTGTATG	NM_001144917.2:c.749-3931_749-3930insTGTGTATG	NM_001144917.2:c.749-3931_749-3930insTGTGTGTATG	NM_001144917.2:c.749-3931_749-3930insTGTGTGTGTATG	NM_001144917.2:c.749-3931_749-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 8	NM_001144918.1:c.404-3931=	NM_001144918.1:c.404-3931_404-3930insTG	NM_001144918.1:c.404-3931_404-3930insTGTG	NM_001144918.1:c.404-3931_404-3930insTGTGTG	NM_001144918.1:c.404-3931_404-3930insTGTGTGTG	NM_001144918.1:c.404-3931_404-3930insTGTGTGTGTG	NM_001144918.1:c.404-3931_404-3930insTGTGTGTGTGTG	NM_001144918.1:c.404-3931_404-3930insTGTGTGTGTGTGTG	NM_001144918.1:c.404-3931_404-3930insTGTATG	NM_001144918.1:c.404-3931_404-3930insTGTGTATG	NM_001144918.1:c.404-3931_404-3930insTGTGTGTATG	NM_001144918.1:c.404-3931_404-3930insTGTGTGTGTATG	NM_001144918.1:c.404-3931_404-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 8	NM_001144918.2:c.404-3931=	NM_001144918.2:c.404-3931_404-3930insTG	NM_001144918.2:c.404-3931_404-3930insTGTG	NM_001144918.2:c.404-3931_404-3930insTGTGTG	NM_001144918.2:c.404-3931_404-3930insTGTGTGTG	NM_001144918.2:c.404-3931_404-3930insTGTGTGTGTG	NM_001144918.2:c.404-3931_404-3930insTGTGTGTGTGTG	NM_001144918.2:c.404-3931_404-3930insTGTGTGTGTGTGTG	NM_001144918.2:c.404-3931_404-3930insTGTATG	NM_001144918.2:c.404-3931_404-3930insTGTGTATG	NM_001144918.2:c.404-3931_404-3930insTGTGTGTATG	NM_001144918.2:c.404-3931_404-3930insTGTGTGTGTATG	NM_001144918.2:c.404-3931_404-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 9	NM_001144919.1:c.482-3931=	NM_001144919.1:c.482-3931_482-3930insTG	NM_001144919.1:c.482-3931_482-3930insTGTG	NM_001144919.1:c.482-3931_482-3930insTGTGTG	NM_001144919.1:c.482-3931_482-3930insTGTGTGTG	NM_001144919.1:c.482-3931_482-3930insTGTGTGTGTG	NM_001144919.1:c.482-3931_482-3930insTGTGTGTGTGTG	NM_001144919.1:c.482-3931_482-3930insTGTGTGTGTGTGTG	NM_001144919.1:c.482-3931_482-3930insTGTATG	NM_001144919.1:c.482-3931_482-3930insTGTGTATG	NM_001144919.1:c.482-3931_482-3930insTGTGTGTATG	NM_001144919.1:c.482-3931_482-3930insTGTGTGTGTATG	NM_001144919.1:c.482-3931_482-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 9	NM_001144919.2:c.482-3931=	NM_001144919.2:c.482-3931_482-3930insTG	NM_001144919.2:c.482-3931_482-3930insTGTG	NM_001144919.2:c.482-3931_482-3930insTGTGTG	NM_001144919.2:c.482-3931_482-3930insTGTGTGTG	NM_001144919.2:c.482-3931_482-3930insTGTGTGTGTG	NM_001144919.2:c.482-3931_482-3930insTGTGTGTGTGTG	NM_001144919.2:c.482-3931_482-3930insTGTGTGTGTGTGTG	NM_001144919.2:c.482-3931_482-3930insTGTATG	NM_001144919.2:c.482-3931_482-3930insTGTGTATG	NM_001144919.2:c.482-3931_482-3930insTGTGTGTATG	NM_001144919.2:c.482-3931_482-3930insTGTGTGTGTATG	NM_001144919.2:c.482-3931_482-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 15	NM_001320654.2:c.64+2055=	NM_001320654.2:c.64+2055_64+2056insTG	NM_001320654.2:c.64+2055_64+2056insTGTG	NM_001320654.2:c.64+2055_64+2056insTGTGTG	NM_001320654.2:c.64+2055_64+2056insTGTGTGTG	NM_001320654.2:c.64+2055_64+2056insTGTGTGTGTG	NM_001320654.2:c.64+2055_64+2056insTGTGTGTGTGTG	NM_001320654.2:c.64+2055_64+2056insTGTGTGTGTGTGTG	NM_001320654.2:c.64+2055_64+2056insTGTATG	NM_001320654.2:c.64+2055_64+2056insTGTGTATG	NM_001320654.2:c.64+2055_64+2056insTGTGTGTATG	NM_001320654.2:c.64+2055_64+2056insTGTGTGTGTATG	NM_001320654.2:c.64+2055_64+2056insTGTGTGTGTGTATG
FGFR2 transcript variant 16	NM_001320658.2:c.749-3931=	NM_001320658.2:c.749-3931_749-3930insTG	NM_001320658.2:c.749-3931_749-3930insTGTG	NM_001320658.2:c.749-3931_749-3930insTGTGTG	NM_001320658.2:c.749-3931_749-3930insTGTGTGTG	NM_001320658.2:c.749-3931_749-3930insTGTGTGTGTG	NM_001320658.2:c.749-3931_749-3930insTGTGTGTGTGTG	NM_001320658.2:c.749-3931_749-3930insTGTGTGTGTGTGTG	NM_001320658.2:c.749-3931_749-3930insTGTATG	NM_001320658.2:c.749-3931_749-3930insTGTGTATG	NM_001320658.2:c.749-3931_749-3930insTGTGTGTATG	NM_001320658.2:c.749-3931_749-3930insTGTGTGTGTATG	NM_001320658.2:c.749-3931_749-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 2	NM_022970.3:c.749-3931=	NM_022970.3:c.749-3931_749-3930insTG	NM_022970.3:c.749-3931_749-3930insTGTG	NM_022970.3:c.749-3931_749-3930insTGTGTG	NM_022970.3:c.749-3931_749-3930insTGTGTGTG	NM_022970.3:c.749-3931_749-3930insTGTGTGTGTG	NM_022970.3:c.749-3931_749-3930insTGTGTGTGTGTG	NM_022970.3:c.749-3931_749-3930insTGTGTGTGTGTGTG	NM_022970.3:c.749-3931_749-3930insTGTATG	NM_022970.3:c.749-3931_749-3930insTGTGTATG	NM_022970.3:c.749-3931_749-3930insTGTGTGTATG	NM_022970.3:c.749-3931_749-3930insTGTGTGTGTATG	NM_022970.3:c.749-3931_749-3930insTGTGTGTGTGTATG
FGFR2 transcript variant 11	NM_023029.2:c.482-3931=	NM_023029.2:c.482-3931_482-3930insTG	NM_023029.2:c.482-3931_482-3930insTGTG	NM_023029.2:c.482-3931_482-3930insTGTGTG	NM_023029.2:c.482-3931_482-3930insTGTGTGTG	NM_023029.2:c.482-3931_482-3930insTGTGTGTGTG	NM_023029.2:c.482-3931_482-3930insTGTGTGTGTGTG	NM_023029.2:c.482-3931_482-3930insTGTGTGTGTGTGTG	NM_023029.2:c.482-3931_482-3930insTGTATG	NM_023029.2:c.482-3931_482-3930insTGTGTATG	NM_023029.2:c.482-3931_482-3930insTGTGTGTATG	NM_023029.2:c.482-3931_482-3930insTGTGTGTGTATG	NM_023029.2:c.482-3931_482-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X1	XM_006717708.4:c.806-3931=	XM_006717708.4:c.806-3931_806-3930insTG	XM_006717708.4:c.806-3931_806-3930insTGTG	XM_006717708.4:c.806-3931_806-3930insTGTGTG	XM_006717708.4:c.806-3931_806-3930insTGTGTGTG	XM_006717708.4:c.806-3931_806-3930insTGTGTGTGTG	XM_006717708.4:c.806-3931_806-3930insTGTGTGTGTGTG	XM_006717708.4:c.806-3931_806-3930insTGTGTGTGTGTGTG	XM_006717708.4:c.806-3931_806-3930insTGTATG	XM_006717708.4:c.806-3931_806-3930insTGTGTATG	XM_006717708.4:c.806-3931_806-3930insTGTGTGTATG	XM_006717708.4:c.806-3931_806-3930insTGTGTGTGTATG	XM_006717708.4:c.806-3931_806-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X2	XM_006717710.5:c.806-3931=	XM_006717710.5:c.806-3931_806-3930insTG	XM_006717710.5:c.806-3931_806-3930insTGTG	XM_006717710.5:c.806-3931_806-3930insTGTGTG	XM_006717710.5:c.806-3931_806-3930insTGTGTGTG	XM_006717710.5:c.806-3931_806-3930insTGTGTGTGTG	XM_006717710.5:c.806-3931_806-3930insTGTGTGTGTGTG	XM_006717710.5:c.806-3931_806-3930insTGTGTGTGTGTGTG	XM_006717710.5:c.806-3931_806-3930insTGTATG	XM_006717710.5:c.806-3931_806-3930insTGTGTATG	XM_006717710.5:c.806-3931_806-3930insTGTGTGTATG	XM_006717710.5:c.806-3931_806-3930insTGTGTGTGTATG	XM_006717710.5:c.806-3931_806-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X3	XM_017015920.3:c.806-3931=	XM_017015920.3:c.806-3931_806-3930insTG	XM_017015920.3:c.806-3931_806-3930insTGTG	XM_017015920.3:c.806-3931_806-3930insTGTGTG	XM_017015920.3:c.806-3931_806-3930insTGTGTGTG	XM_017015920.3:c.806-3931_806-3930insTGTGTGTGTG	XM_017015920.3:c.806-3931_806-3930insTGTGTGTGTGTG	XM_017015920.3:c.806-3931_806-3930insTGTGTGTGTGTGTG	XM_017015920.3:c.806-3931_806-3930insTGTATG	XM_017015920.3:c.806-3931_806-3930insTGTGTATG	XM_017015920.3:c.806-3931_806-3930insTGTGTGTATG	XM_017015920.3:c.806-3931_806-3930insTGTGTGTGTATG	XM_017015920.3:c.806-3931_806-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X4	XM_017015921.3:c.806-3931=	XM_017015921.3:c.806-3931_806-3930insTG	XM_017015921.3:c.806-3931_806-3930insTGTG	XM_017015921.3:c.806-3931_806-3930insTGTGTG	XM_017015921.3:c.806-3931_806-3930insTGTGTGTG	XM_017015921.3:c.806-3931_806-3930insTGTGTGTGTG	XM_017015921.3:c.806-3931_806-3930insTGTGTGTGTGTG	XM_017015921.3:c.806-3931_806-3930insTGTGTGTGTGTGTG	XM_017015921.3:c.806-3931_806-3930insTGTATG	XM_017015921.3:c.806-3931_806-3930insTGTGTATG	XM_017015921.3:c.806-3931_806-3930insTGTGTGTATG	XM_017015921.3:c.806-3931_806-3930insTGTGTGTGTATG	XM_017015921.3:c.806-3931_806-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X10	XM_017015924.3:c.461-3931=	XM_017015924.3:c.461-3931_461-3930insTG	XM_017015924.3:c.461-3931_461-3930insTGTG	XM_017015924.3:c.461-3931_461-3930insTGTGTG	XM_017015924.3:c.461-3931_461-3930insTGTGTGTG	XM_017015924.3:c.461-3931_461-3930insTGTGTGTGTG	XM_017015924.3:c.461-3931_461-3930insTGTGTGTGTGTG	XM_017015924.3:c.461-3931_461-3930insTGTGTGTGTGTGTG	XM_017015924.3:c.461-3931_461-3930insTGTATG	XM_017015924.3:c.461-3931_461-3930insTGTGTATG	XM_017015924.3:c.461-3931_461-3930insTGTGTGTATG	XM_017015924.3:c.461-3931_461-3930insTGTGTGTGTATG	XM_017015924.3:c.461-3931_461-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X11	XM_017015925.3:c.461-3931=	XM_017015925.3:c.461-3931_461-3930insTG	XM_017015925.3:c.461-3931_461-3930insTGTG	XM_017015925.3:c.461-3931_461-3930insTGTGTG	XM_017015925.3:c.461-3931_461-3930insTGTGTGTG	XM_017015925.3:c.461-3931_461-3930insTGTGTGTGTG	XM_017015925.3:c.461-3931_461-3930insTGTGTGTGTGTG	XM_017015925.3:c.461-3931_461-3930insTGTGTGTGTGTGTG	XM_017015925.3:c.461-3931_461-3930insTGTATG	XM_017015925.3:c.461-3931_461-3930insTGTGTATG	XM_017015925.3:c.461-3931_461-3930insTGTGTGTATG	XM_017015925.3:c.461-3931_461-3930insTGTGTGTGTATG	XM_017015925.3:c.461-3931_461-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X6	XM_024447887.2:c.539-3931=	XM_024447887.2:c.539-3931_539-3930insTG	XM_024447887.2:c.539-3931_539-3930insTGTG	XM_024447887.2:c.539-3931_539-3930insTGTGTG	XM_024447887.2:c.539-3931_539-3930insTGTGTGTG	XM_024447887.2:c.539-3931_539-3930insTGTGTGTGTG	XM_024447887.2:c.539-3931_539-3930insTGTGTGTGTGTG	XM_024447887.2:c.539-3931_539-3930insTGTGTGTGTGTGTG	XM_024447887.2:c.539-3931_539-3930insTGTATG	XM_024447887.2:c.539-3931_539-3930insTGTGTATG	XM_024447887.2:c.539-3931_539-3930insTGTGTGTATG	XM_024447887.2:c.539-3931_539-3930insTGTGTGTGTATG	XM_024447887.2:c.539-3931_539-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X7	XM_024447888.2:c.539-3931=	XM_024447888.2:c.539-3931_539-3930insTG	XM_024447888.2:c.539-3931_539-3930insTGTG	XM_024447888.2:c.539-3931_539-3930insTGTGTG	XM_024447888.2:c.539-3931_539-3930insTGTGTGTG	XM_024447888.2:c.539-3931_539-3930insTGTGTGTGTG	XM_024447888.2:c.539-3931_539-3930insTGTGTGTGTGTG	XM_024447888.2:c.539-3931_539-3930insTGTGTGTGTGTGTG	XM_024447888.2:c.539-3931_539-3930insTGTATG	XM_024447888.2:c.539-3931_539-3930insTGTGTATG	XM_024447888.2:c.539-3931_539-3930insTGTGTGTATG	XM_024447888.2:c.539-3931_539-3930insTGTGTGTGTATG	XM_024447888.2:c.539-3931_539-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X8	XM_024447889.2:c.539-3931=	XM_024447889.2:c.539-3931_539-3930insTG	XM_024447889.2:c.539-3931_539-3930insTGTG	XM_024447889.2:c.539-3931_539-3930insTGTGTG	XM_024447889.2:c.539-3931_539-3930insTGTGTGTG	XM_024447889.2:c.539-3931_539-3930insTGTGTGTGTG	XM_024447889.2:c.539-3931_539-3930insTGTGTGTGTGTG	XM_024447889.2:c.539-3931_539-3930insTGTGTGTGTGTGTG	XM_024447889.2:c.539-3931_539-3930insTGTATG	XM_024447889.2:c.539-3931_539-3930insTGTGTATG	XM_024447889.2:c.539-3931_539-3930insTGTGTGTATG	XM_024447889.2:c.539-3931_539-3930insTGTGTGTGTATG	XM_024447889.2:c.539-3931_539-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X5	XM_024447890.2:c.539-3931=	XM_024447890.2:c.539-3931_539-3930insTG	XM_024447890.2:c.539-3931_539-3930insTGTG	XM_024447890.2:c.539-3931_539-3930insTGTGTG	XM_024447890.2:c.539-3931_539-3930insTGTGTGTG	XM_024447890.2:c.539-3931_539-3930insTGTGTGTGTG	XM_024447890.2:c.539-3931_539-3930insTGTGTGTGTGTG	XM_024447890.2:c.539-3931_539-3930insTGTGTGTGTGTGTG	XM_024447890.2:c.539-3931_539-3930insTGTATG	XM_024447890.2:c.539-3931_539-3930insTGTGTATG	XM_024447890.2:c.539-3931_539-3930insTGTGTGTATG	XM_024447890.2:c.539-3931_539-3930insTGTGTGTGTATG	XM_024447890.2:c.539-3931_539-3930insTGTGTGTGTGTATG
FGFR2 transcript variant X9	XM_024447891.2:c.461-3931=	XM_024447891.2:c.461-3931_461-3930insTG	XM_024447891.2:c.461-3931_461-3930insTGTG	XM_024447891.2:c.461-3931_461-3930insTGTGTG	XM_024447891.2:c.461-3931_461-3930insTGTGTGTG	XM_024447891.2:c.461-3931_461-3930insTGTGTGTGTG	XM_024447891.2:c.461-3931_461-3930insTGTGTGTGTGTG	XM_024447891.2:c.461-3931_461-3930insTGTGTGTGTGTGTG	XM_024447891.2:c.461-3931_461-3930insTGTATG	XM_024447891.2:c.461-3931_461-3930insTGTGTATG	XM_024447891.2:c.461-3931_461-3930insTGTGTGTATG	XM_024447891.2:c.461-3931_461-3930insTGTGTGTGTATG	XM_024447891.2:c.461-3931_461-3930insTGTGTGTGTGTATG

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#.

9 SubSNP, 8 Frequency submissions

No	Submitter	Submission ID	Date (Build)
1	DDI	ss1536672071	Jan 10, 2018 (151)
2	EVA_DECODE	ss3690835803	Jul 13, 2019 (153)
3	GNOMAD	ss4227020010	Apr 26, 2021 (155)
4	GNOMAD	ss4227020011	Apr 26, 2021 (155)
5	GNOMAD	ss4227020012	Apr 26, 2021 (155)
6	GNOMAD	ss4227020013	Apr 26, 2021 (155)
7	GNOMAD	ss4227020014	Apr 26, 2021 (155)
8	GNOMAD	ss4227020015	Apr 26, 2021 (155)
9	GNOMAD	ss4227020016	Apr 26, 2021 (155)
10	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366211826 (NC_000010.11:121524099::AC 1037/126300) Row 366211827 (NC_000010.11:121524099::ACAC 615/126266) Row 366211828 (NC_000010.11:121524099::ACACAC 124/126334)...	-	Apr 26, 2021 (155)
11	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366211826 (NC_000010.11:121524099::AC 1037/126300) Row 366211827 (NC_000010.11:121524099::ACAC 615/126266) Row 366211828 (NC_000010.11:121524099::ACACAC 124/126334)...	-	Apr 26, 2021 (155)
12	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366211826 (NC_000010.11:121524099::AC 1037/126300) Row 366211827 (NC_000010.11:121524099::ACAC 615/126266) Row 366211828 (NC_000010.11:121524099::ACACAC 124/126334)...	-	Apr 26, 2021 (155)
13	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366211826 (NC_000010.11:121524099::AC 1037/126300) Row 366211827 (NC_000010.11:121524099::ACAC 615/126266) Row 366211828 (NC_000010.11:121524099::ACACAC 124/126334)...	-	Apr 26, 2021 (155)
14	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366211826 (NC_000010.11:121524099::AC 1037/126300) Row 366211827 (NC_000010.11:121524099::ACAC 615/126266) Row 366211828 (NC_000010.11:121524099::ACACAC 124/126334)...	-	Apr 26, 2021 (155)
15	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366211826 (NC_000010.11:121524099::AC 1037/126300) Row 366211827 (NC_000010.11:121524099::ACAC 615/126266) Row 366211828 (NC_000010.11:121524099::ACACAC 124/126334)...	-	Apr 26, 2021 (155)
16	gnomAD - Genomes Submission ignored due to conflicting rows: Row 366211826 (NC_000010.11:121524099::AC 1037/126300) Row 366211827 (NC_000010.11:121524099::ACAC 615/126266) Row 366211828 (NC_000010.11:121524099::ACACAC 124/126334)...	-	Apr 26, 2021 (155)
17	ALFA	NC_000010.11 - 121524100	Apr 26, 2021 (155)

History tab displays RefSNPs (Associated ID) from previous builds (Build) that now support the current RefSNP, and the dates, when the history was updated for each Associated ID (History Updated).

Added to this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI	Source RSIDs
ss1536672071	NC_000010.10:123283613::AC	NC_000010.11:121524099:A:ACA	(self)
ss4227020010	NC_000010.11:121524099::AC	NC_000010.11:121524099:A:ACA	(self)
1921577063	NC_000010.11:121524099:A:ACA	NC_000010.11:121524099:A:ACA	(self)
ss3690835803	NC_000010.11:121524100::CA	NC_000010.11:121524099:A:ACA	(self)
ss4227020011	NC_000010.11:121524099::ACAC	NC_000010.11:121524099:A:ACACA	(self)
1921577063	NC_000010.11:121524099:A:ACACA	NC_000010.11:121524099:A:ACACA	(self)
ss4227020012	NC_000010.11:121524099::ACACAC	NC_000010.11:121524099:A:ACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACACACA	NC_000010.11:121524099:A:ACACACA	(self)
ss4227020013	NC_000010.11:121524099::ACACACAC	NC_000010.11:121524099:A:ACACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACACACACA	NC_000010.11:121524099:A:ACACACACA	(self)
ss4227020014	NC_000010.11:121524099::ACACACACAC	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACA	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACA	(self)
ss4227020015	NC_000010.11:121524099::ACACACACAC… NC_000010.11:121524099::ACACACACACAC	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACACA	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACACA	(self)
ss4227020016	NC_000010.11:121524099::ACACACACAC… NC_000010.11:121524099::ACACACACACACAC	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACACACA	NC_000010.11:121524099:A:ACACACACA… NC_000010.11:121524099:A:ACACACACACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACATACA	NC_000010.11:121524099:A:ACATACA	(self)
1921577063	NC_000010.11:121524099:A:ACATACACA	NC_000010.11:121524099:A:ACATACACA	(self)
1921577063	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACA	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACACA	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACACA	(self)
1921577063	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACACACA	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACACACA	(self)

Removed from this RefSNP Cluster:

Submission IDs	Observation SPDI	Canonical SPDI
ss3132432733	NC_000010.11:121524099::ACATAC	NC_000010.11:121524099:A:ACATACA
ss3132432734	NC_000010.11:121524099::ACATACAC	NC_000010.11:121524099:A:ACATACACA
ss3132432735	NC_000010.11:121524099::ACATACACAC	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACA
ss3132432736	NC_000010.11:121524099::ACATACACAC… NC_000010.11:121524099::ACATACACACAC	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACACA
ss3132432737	NC_000010.11:121524099::ACATACACAC… NC_000010.11:121524099::ACATACACACACAC	NC_000010.11:121524099:A:ACATACACA… NC_000010.11:121524099:A:ACATACACACACACA

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

No publications for rs1491543645

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
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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.
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dbSNP Short Genetic Variations

Welcome to the Reference SNP (rs) Report

Reference SNP (rs) Report

rs1491543645