SNP Links for Gene (Select 994) - SNP

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Select item 14914235121.

rs1491423512 has merged into rs758801099 [Homo sapiens]

Variant type:: DELINS
Alleles:: AA>-,A,AAA,AAAA,AAAAA [Show Flanks]
Chromosome:: 20:3795375 (GRCh38)
20:3776022 (GRCh37)
Canonical SPDI:: NC_000020.11:3795372:AAAA:AA,NC_000020.11:3795372:AAAA:AAA,NC_000020.11:3795372:AAAA:AAAAA,NC_000020.11:3795372:AAAA:AAAAAA,NC_000020.11:3795372:AAAA:AAAAAAA
Gene:: CDC25B (Varview)
Functional Consequence:: upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAA=0./0 (ALFA)
-=0.00284/4 (Korea1K)
-=0.00839/99 (TOMMO)
-=0.025/1 (GENOME_DK)
HGVS:: NC_000020.11:g.3795375_3795376del, NC_000020.11:g.3795376del, NC_000020.11:g.3795376dup, NC_000020.11:g.3795375_3795376dup, NC_000020.11:g.3795374_3795376dup, NC_000020.10:g.3776022_3776023del, NC_000020.10:g.3776023del, NC_000020.10:g.3776023dup, NC_000020.10:g.3776022_3776023dup, NC_000020.10:g.3776021_3776023dup, NG_029040.2:g.13604_13605del, NG_029040.2:g.13605del, NG_029040.2:g.13605dup, NG_029040.2:g.13604_13605dup, NG_029040.2:g.13603_13605dup

Select item 14913408952.

rs1491340895 has merged into rs35316200 [Homo sapiens]

Variant type:: DELINS
Alleles:: CGCGCGCG>-,CG,CGCG,CGCGCG,CGCGCGCGCG,CGCGCGCGCGCG,CGCGCGCGCGCGCG,CGCGCGCGCGCGCGCG,CGCGCGCGCGCGCGCGCG,CGCGCGCGCGCGCGCGCGCG,CGCGCGCGCGCGCGCGCGCGCG [Show Flanks]
Chromosome:: 20:3799531 (GRCh38)
20:3780178 (GRCh37)
Canonical SPDI:: NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCGCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCGCGCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCGCGCGCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCGCGCGCGCGCGCGCG,NC_000020.11:3799525:GCGCGCGCGCGCG:GCGCGCGCGCGCGCGCGCGCGCGCGCG
Gene:: CDC25B (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GCGCGCG=0./0 (ALFA)
GCGC=0.00475/79 (TOMMO)
HGVS:: NC_000020.11:g.3799527CG[2], NC_000020.11:g.3799527CG[3], NC_000020.11:g.3799527CG[4], NC_000020.11:g.3799527CG[5], NC_000020.11:g.3799527CG[7], NC_000020.11:g.3799527CG[8], NC_000020.11:g.3799527CG[9], NC_000020.11:g.3799527CG[10], NC_000020.11:g.3799527CG[11], NC_000020.11:g.3799527CG[12], NC_000020.11:g.3799527CG[13], NC_000020.10:g.3780174CG[2], NC_000020.10:g.3780174CG[3], NC_000020.10:g.3780174CG[4], NC_000020.10:g.3780174CG[5], NC_000020.10:g.3780174CG[7], NC_000020.10:g.3780174CG[8], NC_000020.10:g.3780174CG[9], NC_000020.10:g.3780174CG[10], NC_000020.10:g.3780174CG[11], NC_000020.10:g.3780174CG[12], NC_000020.10:g.3780174CG[13], NG_029040.2:g.17756CG[2], NG_029040.2:g.17756CG[3], NG_029040.2:g.17756CG[4], NG_029040.2:g.17756CG[5], NG_029040.2:g.17756CG[7], NG_029040.2:g.17756CG[8], NG_029040.2:g.17756CG[9], NG_029040.2:g.17756CG[10], NG_029040.2:g.17756CG[11], NG_029040.2:g.17756CG[12], NG_029040.2:g.17756CG[13], NG_060729.1:g.166CG[2], NG_060729.1:g.166CG[3], NG_060729.1:g.166CG[4], NG_060729.1:g.166CG[5], NG_060729.1:g.166CG[7], NG_060729.1:g.166CG[8], NG_060729.1:g.166CG[9], NG_060729.1:g.166CG[10], NG_060729.1:g.166CG[11], NG_060729.1:g.166CG[12], NG_060729.1:g.166CG[13]

Select item 14913176043.

rs1491317604 has merged into rs199903902 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 20:3795377 (GRCh38)
20:3776024 (GRCh37)
Canonical SPDI:: NC_000020.11:3795375:ACA:A
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00169/20 (ALFA)
-=0.0178/66 (TWINSUK)
-=0.02828/109 (ALSPAC)
HGVS:: NC_000020.11:g.3795377_3795378del, NC_000020.10:g.3776024_3776025del, NG_029040.2:g.13606_13607del

Select item 14912593464.

rs1491259346 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 20:3790261 (GRCh38)
20:3770908 (GRCh37)
Canonical SPDI:: NC_000020.11:3790258:CTCT:CT
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
-=0.000035/1 (TOMMO)
HGVS:: NC_000020.11:g.3790259CT[1], NC_000020.10:g.3770906CT[1], NG_029040.2:g.8488CT[1]

Select item 14912109495.

rs1491210949 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTCT [Show Flanks]
Chromosome:: 20:3790259 (GRCh38)
20:3770907 (GRCh37)
Canonical SPDI:: NC_000020.11:3790259:TCTGTCT:TCTGTCTGTCT
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TCTGTCTGTCT=0./0 (ALFA)
TCTG=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.3790263_3790266dup, NC_000020.10:g.3770910_3770913dup, NG_029040.2:g.8492_8495dup

Select item 14911870916.

rs1491187091 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AC [Show Flanks]
Chromosome:: 20:3799526 (GRCh38)
20:3780174 (GRCh37)
Canonical SPDI:: NC_000020.11:3799526:C:CAC
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: CAC=0./0 (ALFA)
CA=0.00005/2 (GnomAD)
HGVS:: NC_000020.11:g.3799527_3799528insAC, NC_000020.10:g.3780174_3780175insAC, NG_029040.2:g.17756_17757insAC, NG_060729.1:g.166_167insAC

Select item 14911822517.

rs1491182251 has merged into rs58192077 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,T,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 20:3798326 (GRCh38)
20:3778973 (GRCh37)
Canonical SPDI:: NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000020.11:3798315:TTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: CDC25B (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
TTTTT=0.4517/2262 (1000Genomes)
HGVS:: NC_000020.11:g.3798326_3798337del, NC_000020.11:g.3798327_3798337del, NC_000020.11:g.3798330_3798337del, NC_000020.11:g.3798331_3798337del, NC_000020.11:g.3798332_3798337del, NC_000020.11:g.3798333_3798337del, NC_000020.11:g.3798334_3798337del, NC_000020.11:g.3798335_3798337del, NC_000020.11:g.3798336_3798337del, NC_000020.11:g.3798337del, NC_000020.11:g.3798337dup, NC_000020.11:g.3798336_3798337dup, NC_000020.11:g.3798335_3798337dup, NC_000020.11:g.3798334_3798337dup, NC_000020.11:g.3798332_3798337dup, NC_000020.11:g.3798331_3798337dup, NC_000020.11:g.3798330_3798337dup, NC_000020.10:g.3778973_3778984del, NC_000020.10:g.3778974_3778984del, NC_000020.10:g.3778977_3778984del, NC_000020.10:g.3778978_3778984del, NC_000020.10:g.3778979_3778984del, NC_000020.10:g.3778980_3778984del, NC_000020.10:g.3778981_3778984del, NC_000020.10:g.3778982_3778984del, NC_000020.10:g.3778983_3778984del, NC_000020.10:g.3778984del, NC_000020.10:g.3778984dup, NC_000020.10:g.3778983_3778984dup, NC_000020.10:g.3778982_3778984dup, NC_000020.10:g.3778981_3778984dup, NC_000020.10:g.3778979_3778984dup, NC_000020.10:g.3778978_3778984dup, NC_000020.10:g.3778977_3778984dup, NG_029040.2:g.16555_16566del, NG_029040.2:g.16556_16566del, NG_029040.2:g.16559_16566del, NG_029040.2:g.16560_16566del, NG_029040.2:g.16561_16566del, NG_029040.2:g.16562_16566del, NG_029040.2:g.16563_16566del, NG_029040.2:g.16564_16566del, NG_029040.2:g.16565_16566del, NG_029040.2:g.16566del, NG_029040.2:g.16566dup, NG_029040.2:g.16565_16566dup, NG_029040.2:g.16564_16566dup, NG_029040.2:g.16563_16566dup, NG_029040.2:g.16561_16566dup, NG_029040.2:g.16560_16566dup, NG_029040.2:g.16559_16566dup

Select item 14910958608.

rs1491095860 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CA [Show Flanks]
Chromosome:: 20:3795373 (GRCh38)
20:3776021 (GRCh37)
Canonical SPDI:: NC_000020.11:3795373:A:ACA
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: ACA=0./0 (ALFA)
HGVS:: NC_000020.11:g.3795374_3795375insCA, NC_000020.10:g.3776021_3776022insCA, NG_029040.2:g.13603_13604insCA

Select item 14910952539.

rs1491095253 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 20:3787029 (GRCh38)
20:3767677 (GRCh37)
Canonical SPDI:: NC_000020.11:3787029:G:GG
Gene:: CDC25B (Varview), CENPB (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,5_prime_UTR_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
G=0.000026/7 (TOPMED)
G=0.00004/5 (GnomAD)
HGVS:: NC_000020.11:g.3787030dup, NC_000020.10:g.3767677dup, NG_029040.2:g.5259dup, NR_136336.2:n.80dup, NR_136336.1:n.259dup, NM_001287516.2:c.-102dup, NM_001287516.1:c.-102dup, NM_001287517.2:c.-102dup, NM_001287517.1:c.-102dup, NM_001287518.2:c.-102dup, NM_001287518.1:c.-102dup

Select item 149093029610.

rs1490930296 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 20:3787370 (GRCh38)
20:3768017 (GRCh37)
Canonical SPDI:: NC_000020.11:3787369:T:A
Gene:: CDC25B (Varview), CENPB (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.3787370T>A, NC_000020.10:g.3768017T>A, NG_029040.2:g.5599T>A

Select item 149078322311.

rs1490783223 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 20:3797695 (GRCh38)
20:3778342 (GRCh37)
Canonical SPDI:: NC_000020.11:3797694:C:A,NC_000020.11:3797694:C:G
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,coding_sequence_variant,5_prime_UTR_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000031/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.3797695C>A, NC_000020.11:g.3797695C>G, NC_000020.10:g.3778342C>A, NC_000020.10:g.3778342C>G, NG_029040.2:g.15924C>A, NG_029040.2:g.15924C>G, NM_004358.5:c.232C>A, NM_004358.5:c.232C>G, NM_004358.4:c.232C>A, NM_004358.4:c.232C>G, NM_004358.3:c.232C>A, NM_004358.3:c.232C>G, NM_021873.4:c.274C>A, NM_021873.4:c.274C>G, NM_021873.3:c.274C>A, NM_021873.3:c.274C>G, NM_021873.2:c.274C>A, NM_021873.2:c.274C>G, NM_021872.4:c.274C>A, NM_021872.4:c.274C>G, NM_021872.3:c.274C>A, NM_021872.3:c.274C>G, NM_021872.2:c.274C>A, NM_021872.2:c.274C>G, NR_136336.2:n.263C>A, NR_136336.2:n.263C>G, NR_136336.1:n.442C>A, NR_136336.1:n.442C>G, NM_001287516.2:c.82C>A, NM_001287516.2:c.82C>G, NM_001287516.1:c.82C>A, NM_001287516.1:c.82C>G, NR_136335.2:n.165C>A, NR_136335.2:n.165C>G, NR_136335.1:n.215C>A, NR_136335.1:n.215C>G, NM_001287517.2:c.40C>A, NM_001287517.2:c.40C>G, NM_001287517.1:c.40C>A, NM_001287517.1:c.40C>G, NM_001287518.2:c.82C>A, NM_001287518.2:c.82C>G, NM_001287518.1:c.82C>A, NM_001287518.1:c.82C>G, NM_001287520.2:c.-63C>A, NM_001287520.2:c.-63C>G, NM_001287520.1:c.-63C>A, NM_001287520.1:c.-63C>G, NM_001287519.2:c.-63C>A, NM_001287519.2:c.-63C>G, NM_001287519.1:c.-63C>A, NM_001287519.1:c.-63C>G, NM_001287522.2:c.-63C>A, NM_001287522.2:c.-63C>G, NM_001287522.1:c.-63C>A, NM_001287522.1:c.-63C>G, NM_021874.2:c.232C>A, NM_021874.2:c.232C>G, NM_021874.1:c.232C>A, NM_021874.1:c.232C>G, NM_212530.1:c.-63C>A, NM_212530.1:c.-63C>G, XM_047440628.1:c.274C>A, XM_047440628.1:c.274C>G, NP_004349.1:p.Arg78Gly, NP_068659.1:p.Arg92Gly, NP_068658.1:p.Arg92Gly, NP_001274445.1:p.Arg28Gly, NP_001274446.1:p.Arg14Gly, NP_001274447.1:p.Arg28Gly, XP_047296584.1:p.Arg92Gly

Select item 149071532512.

rs1490715325 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:3788380 (GRCh38)
20:3769027 (GRCh37)
Canonical SPDI:: NC_000020.11:3788379:T:C
Gene:: CDC25B (Varview), CENPB (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.3788380T>C, NC_000020.10:g.3769027T>C, NG_029040.2:g.6609T>C

Select item 149061785613.

rs1490617856 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 20:3795754 (GRCh38)
20:3776401 (GRCh37)
Canonical SPDI:: NC_000020.11:3795753:G:T
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.3795754G>T, NC_000020.10:g.3776401G>T, NG_029040.2:g.13983G>T, NM_021873.3:c.-778G>T, NM_004358.4:c.-778G>T, NM_004358.3:c.-778G>T, NM_021872.3:c.-778G>T, NM_021874.2:c.-778G>T, NM_021873.2:c.-778G>T, NM_021872.2:c.-778G>T, NR_136335.1:n.16G>T, NM_001287520.1:c.-262G>T, NM_212530.1:c.-262G>T, NM_001287519.1:c.-220G>T, NM_001287522.1:c.-262G>T

Select item 149043438214.

rs1490434382 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 20:3787964 (GRCh38)
20:3768611 (GRCh37)
Canonical SPDI:: NC_000020.11:3787963:C:A,NC_000020.11:3787963:C:T
Gene:: CDC25B (Varview), CENPB (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000106/2 (TOMMO)
HGVS:: NC_000020.11:g.3787964C>A, NC_000020.11:g.3787964C>T, NC_000020.10:g.3768611C>A, NC_000020.10:g.3768611C>T, NG_029040.2:g.6193C>A, NG_029040.2:g.6193C>T

Select item 149033368015.

rs1490333680 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 20:3798315 (GRCh38)
20:3778962 (GRCh37)
Canonical SPDI:: NC_000020.11:3798314:G:
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00064/18 (TOMMO)
-=0.03047/113 (TWINSUK)
-=0.04203/162 (ALSPAC)
HGVS:: NC_000020.11:g.3798315del, NC_000020.10:g.3778962del, NG_029040.2:g.16544del

Select item 149031880016.

rs1490318800 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 20:3796360 (GRCh38)
20:3777007 (GRCh37)
Canonical SPDI:: NC_000020.11:3796359:T:A,NC_000020.11:3796359:T:C,NC_000020.11:3796359:T:G
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.14313/2337 (ALFA)
C=0.00324/54 (TOMMO)
C=0.01078/19 (Korea1K)
C=0.14386/410 (KOREAN)
HGVS:: NC_000020.11:g.3796360T>A, NC_000020.11:g.3796360T>C, NC_000020.11:g.3796360T>G, NC_000020.10:g.3777007T>A, NC_000020.10:g.3777007T>C, NC_000020.10:g.3777007T>G, NG_029040.2:g.14589T>A, NG_029040.2:g.14589T>C, NG_029040.2:g.14589T>G, NM_004358.5:c.-172T>A, NM_004358.5:c.-172T>C, NM_004358.5:c.-172T>G, NM_004358.4:c.-172T>A, NM_004358.4:c.-172T>C, NM_004358.4:c.-172T>G, NM_004358.3:c.-172T>A, NM_004358.3:c.-172T>C, NM_004358.3:c.-172T>G, NM_021873.4:c.-172T>A, NM_021873.4:c.-172T>C, NM_021873.4:c.-172T>G, NM_021873.3:c.-172T>A, NM_021873.3:c.-172T>C, NM_021873.3:c.-172T>G, NM_021873.2:c.-172T>A, NM_021873.2:c.-172T>C, NM_021873.2:c.-172T>G, NM_021872.4:c.-172T>A, NM_021872.4:c.-172T>C, NM_021872.4:c.-172T>G, NM_021872.3:c.-172T>A, NM_021872.3:c.-172T>C, NM_021872.3:c.-172T>G, NM_021872.2:c.-172T>A, NM_021872.2:c.-172T>C, NM_021872.2:c.-172T>G, NM_021874.2:c.-172T>A, NM_021874.2:c.-172T>C, NM_021874.2:c.-172T>G, NM_021874.1:c.-172T>A, NM_021874.1:c.-172T>C, NM_021874.1:c.-172T>G, XM_047440628.1:c.-172T>A, XM_047440628.1:c.-172T>C, XM_047440628.1:c.-172T>G

Select item 149029234817.

rs1490292348 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:3795095 (GRCh38)
20:3775742 (GRCh37)
Canonical SPDI:: NC_000020.11:3795094:C:T
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000038/10 (TOPMED)
T=0.00005/7 (GnomAD)
T=0.001667/1 (NorthernSweden)
HGVS:: NC_000020.11:g.3795095C>T, NC_000020.10:g.3775742C>T, NG_029040.2:g.13324C>T

Select item 148987162518.

rs1489871625 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 20:3800427 (GRCh38)
20:3781074 (GRCh37)
Canonical SPDI:: NC_000020.11:3800426:T:A
Gene:: CDC25B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.3800427T>A, NC_000020.10:g.3781074T>A, NG_029040.2:g.18656T>A, NG_080888.1:g.26T>A

Select item 148969448019.

rs1489694480 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 20:3794561 (GRCh38)
20:3775209 (GRCh37)
Canonical SPDI:: NC_000020.11:3794561:CCCCC:CCCCCC
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: CCCCCC=0.000084/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.3794566dup, NC_000020.10:g.3775213dup, NG_029040.2:g.12795dup

Select item 148955417520.

rs1489554175 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 20:3797240 (GRCh38)
20:3777887 (GRCh37)
Canonical SPDI:: NC_000020.11:3797239:C:A,NC_000020.11:3797239:C:T
Gene:: CDC25B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.3797240C>A, NC_000020.11:g.3797240C>T, NC_000020.10:g.3777887C>A, NC_000020.10:g.3777887C>T, NG_029040.2:g.15469C>A, NG_029040.2:g.15469C>T

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