SNP Links for Gene (Select 4603) - SNP

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Select item 14914356641.

rs1491435664 has merged into rs1189665191 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 8:66597857 (GRCh38)
8:67510092 (GRCh37)
Canonical SPDI:: NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000008.11:66597847:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000008.11:g.66597857_66597873del, NC_000008.11:g.66597858_66597873del, NC_000008.11:g.66597859_66597873del, NC_000008.11:g.66597860_66597873del, NC_000008.11:g.66597861_66597873del, NC_000008.11:g.66597862_66597873del, NC_000008.11:g.66597864_66597873del, NC_000008.11:g.66597865_66597873del, NC_000008.11:g.66597866_66597873del, NC_000008.11:g.66597867_66597873del, NC_000008.11:g.66597869_66597873del, NC_000008.11:g.66597870_66597873del, NC_000008.11:g.66597871_66597873del, NC_000008.11:g.66597872_66597873del, NC_000008.11:g.66597873del, NC_000008.11:g.66597873dup, NC_000008.11:g.66597872_66597873dup, NC_000008.11:g.66597871_66597873dup, NC_000008.11:g.66597870_66597873dup, NC_000008.11:g.66597868_66597873dup, NC_000008.11:g.66597867_66597873dup, NC_000008.11:g.66597866_66597873dup, NC_000008.11:g.66597865_66597873dup, NC_000008.10:g.67510092_67510108del, NC_000008.10:g.67510093_67510108del, NC_000008.10:g.67510094_67510108del, NC_000008.10:g.67510095_67510108del, NC_000008.10:g.67510096_67510108del, NC_000008.10:g.67510097_67510108del, NC_000008.10:g.67510099_67510108del, NC_000008.10:g.67510100_67510108del, NC_000008.10:g.67510101_67510108del, NC_000008.10:g.67510102_67510108del, NC_000008.10:g.67510104_67510108del, NC_000008.10:g.67510105_67510108del, NC_000008.10:g.67510106_67510108del, NC_000008.10:g.67510107_67510108del, NC_000008.10:g.67510108del, NC_000008.10:g.67510108dup, NC_000008.10:g.67510107_67510108dup, NC_000008.10:g.67510106_67510108dup, NC_000008.10:g.67510105_67510108dup, NC_000008.10:g.67510103_67510108dup, NC_000008.10:g.67510102_67510108dup, NC_000008.10:g.67510101_67510108dup, NC_000008.10:g.67510100_67510108dup

Select item 14913692072.

rs1491369207 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATAA,ATATATATA,ATATATATATA,ATATATATATATA,ATATATATATATATA,ATATATATATATATATATATATATG [Show Flanks]
Chromosome:: 8:66602734 (GRCh38)
8:67514970 (GRCh37)
Canonical SPDI:: NC_000008.11:66602734::A,NC_000008.11:66602734::ATA,NC_000008.11:66602734::ATATA,NC_000008.11:66602734::ATATATA,NC_000008.11:66602734::ATATATAA,NC_000008.11:66602734::ATATATATA,NC_000008.11:66602734::ATATATATATA,NC_000008.11:66602734::ATATATATATATA,NC_000008.11:66602734::ATATATATATATATA,NC_000008.11:66602734::ATATATATATATATATATATATATG
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
HGVS:: NC_000008.11:g.66602734_66602735insA, NC_000008.11:g.66602734_66602735insATA, NC_000008.11:g.66602734_66602735insATATA, NC_000008.11:g.66602734_66602735insATATATA, NC_000008.11:g.66602734_66602735insATATATAA, NC_000008.11:g.66602734_66602735insATATATATA, NC_000008.11:g.66602734_66602735insATATATATATA, NC_000008.11:g.66602734_66602735insATATATATATATA, NC_000008.11:g.66602734_66602735insATATATATATATATA, NC_000008.11:g.66602734_66602735insATATATATATATATATATATATATG, NC_000008.10:g.67514969_67514970insA, NC_000008.10:g.67514969_67514970insATA, NC_000008.10:g.67514969_67514970insATATA, NC_000008.10:g.67514969_67514970insATATATA, NC_000008.10:g.67514969_67514970insATATATAA, NC_000008.10:g.67514969_67514970insATATATATA, NC_000008.10:g.67514969_67514970insATATATATATA, NC_000008.10:g.67514969_67514970insATATATATATATA, NC_000008.10:g.67514969_67514970insATATATATATATATA, NC_000008.10:g.67514969_67514970insATATATATATATATATATATATATG

Select item 14913539513.

rs1491353951 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 8:66591359 (GRCh38)
8:67503594 (GRCh37)
Canonical SPDI:: NC_000008.11:66591358:AT:
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.66591359_66591360del, NC_000008.10:g.67503594_67503595del

Select item 14912398984.

rs1491239898 has merged into rs143426704 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 8:66602748 (GRCh38)
8:67514983 (GRCh37)
Canonical SPDI:: NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:66602733:TTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000008.11:g.66602748_66602761del, NC_000008.11:g.66602749_66602761del, NC_000008.11:g.66602750_66602761del, NC_000008.11:g.66602751_66602761del, NC_000008.11:g.66602752_66602761del, NC_000008.11:g.66602753_66602761del, NC_000008.11:g.66602754_66602761del, NC_000008.11:g.66602755_66602761del, NC_000008.11:g.66602756_66602761del, NC_000008.11:g.66602757_66602761del, NC_000008.11:g.66602758_66602761del, NC_000008.11:g.66602759_66602761del, NC_000008.11:g.66602760_66602761del, NC_000008.11:g.66602761del, NC_000008.11:g.66602761dup, NC_000008.11:g.66602760_66602761dup, NC_000008.11:g.66602759_66602761dup, NC_000008.11:g.66602758_66602761dup, NC_000008.11:g.66602757_66602761dup, NC_000008.11:g.66602756_66602761dup, NC_000008.11:g.66602755_66602761dup, NC_000008.10:g.67514983_67514996del, NC_000008.10:g.67514984_67514996del, NC_000008.10:g.67514985_67514996del, NC_000008.10:g.67514986_67514996del, NC_000008.10:g.67514987_67514996del, NC_000008.10:g.67514988_67514996del, NC_000008.10:g.67514989_67514996del, NC_000008.10:g.67514990_67514996del, NC_000008.10:g.67514991_67514996del, NC_000008.10:g.67514992_67514996del, NC_000008.10:g.67514993_67514996del, NC_000008.10:g.67514994_67514996del, NC_000008.10:g.67514995_67514996del, NC_000008.10:g.67514996del, NC_000008.10:g.67514996dup, NC_000008.10:g.67514995_67514996dup, NC_000008.10:g.67514994_67514996dup, NC_000008.10:g.67514993_67514996dup, NC_000008.10:g.67514992_67514996dup, NC_000008.10:g.67514991_67514996dup, NC_000008.10:g.67514990_67514996dup

Select item 14910942025.

rs1491094202 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 8:66597847 (GRCh38)
8:67510082 (GRCh37)
Canonical SPDI:: NC_000008.11:66597846:TA:
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00084/10 (ALFA)
HGVS:: NC_000008.11:g.66597847_66597848del, NC_000008.10:g.67510082_67510083del

Select item 14909986276.

rs1490998627 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:66581685 (GRCh38)
8:67493920 (GRCh37)
Canonical SPDI:: NC_000008.11:66581684:T:G
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.66581685T>G, NC_000008.10:g.67493920T>G

Select item 14909765897.

rs1490976589 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:66578059 (GRCh38)
8:67490294 (GRCh37)
Canonical SPDI:: NC_000008.11:66578058:C:T
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.66578059C>T, NC_000008.10:g.67490294C>T

Select item 14909531468.

rs1490953146 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 8:66615176 (GRCh38)
8:67527411 (GRCh37)
Canonical SPDI:: NC_000008.11:66615175:T:A,NC_000008.11:66615175:T:C
Gene:: MYBL1 (Varview), LOC105375884 (Varview)
Functional Consequence:: 2KB_upstream_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.66615176T>A, NC_000008.11:g.66615176T>C, NC_000008.10:g.67527411T>A, NC_000008.10:g.67527411T>C, XR_929015.3:n.1236T>A, XR_929015.3:n.1236T>C

Select item 14908831989.

rs1490883198 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 8:66601018 (GRCh38)
8:67513254 (GRCh37)
Canonical SPDI:: NC_000008.11:66601018::G
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000008.11:g.66601018_66601019insG, NC_000008.10:g.67513253_67513254insG

Select item 149086941610.

rs1490869416 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:66582770 (GRCh38)
8:67495005 (GRCh37)
Canonical SPDI:: NC_000008.11:66582769:T:C
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000015/2 (GnomAD)
HGVS:: NC_000008.11:g.66582770T>C, NC_000008.10:g.67495005T>C

Select item 149078252311.

rs1490782523 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:66590148 (GRCh38)
8:67502383 (GRCh37)
Canonical SPDI:: NC_000008.11:66590147:T:C
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_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_000008.11:g.66590148T>C, NC_000008.10:g.67502383T>C

Select item 149057701112.

rs1490577011 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:66574750 (GRCh38)
8:67486985 (GRCh37)
Canonical SPDI:: NC_000008.11:66574749:A:G
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.66574750A>G, NC_000008.10:g.67486985A>G

Select item 149050434813.

rs1490504348 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:66581124 (GRCh38)
8:67493359 (GRCh37)
Canonical SPDI:: NC_000008.11:66581123:A:T
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000008.11:g.66581124A>T, NC_000008.10:g.67493359A>T

Select item 149037675114.

rs1490376751 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:66582487 (GRCh38)
8:67494722 (GRCh37)
Canonical SPDI:: NC_000008.11:66582486:G:T
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000008.11:g.66582487G>T, NC_000008.10:g.67494722G>T

Select item 149018323115.

rs1490183231 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 8:66567760 (GRCh38)
8:67479996 (GRCh37)
Canonical SPDI:: NC_000008.11:66567760:T:TT
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.66567761dup, NC_000008.10:g.67479996dup

Select item 149017931616.

rs1490179316 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 8:66582339 (GRCh38)
8:67494575 (GRCh37)
Canonical SPDI:: NC_000008.11:66582339:AAAAA:AAAAAA
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAA=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.66582344dup, NC_000008.10:g.67494579dup

Select item 149005912017.

rs1490059120 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:66601054 (GRCh38)
8:67513289 (GRCh37)
Canonical SPDI:: NC_000008.11:66601053:G:A
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.66601054G>A, NC_000008.10:g.67513289G>A

Select item 148999899218.

rs1489998992 has merged into rs542129633 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA [Show Flanks]
Chromosome:: 8:66607711 (GRCh38)
8:67519946 (GRCh37)
Canonical SPDI:: NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000008.11:66607699:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.109625/549 (1000Genomes)
-=0.225/9 (GENOME_DK)
HGVS:: NC_000008.11:g.66607711_66607714del, NC_000008.11:g.66607712_66607714del, NC_000008.11:g.66607713_66607714del, NC_000008.11:g.66607714del, NC_000008.11:g.66607714dup, NC_000008.11:g.66607713_66607714dup, NC_000008.11:g.66607712_66607714dup, NC_000008.11:g.66607711_66607714dup, NC_000008.10:g.67519946_67519949del, NC_000008.10:g.67519947_67519949del, NC_000008.10:g.67519948_67519949del, NC_000008.10:g.67519949del, NC_000008.10:g.67519949dup, NC_000008.10:g.67519948_67519949dup, NC_000008.10:g.67519947_67519949dup, NC_000008.10:g.67519946_67519949dup

Select item 148992639619.

rs1489926396 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:66566838 (GRCh38)
8:67479073 (GRCh37)
Canonical SPDI:: NC_000008.11:66566837:C:T
Gene:: MYBL1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.66566838C>T, NC_000008.10:g.67479073C>T

Select item 148989142020.

rs1489891420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:66608820 (GRCh38)
8:67521055 (GRCh37)
Canonical SPDI:: NC_000008.11:66608819:C:G
Gene:: MYBL1 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000008.11:g.66608820C>G, NC_000008.10:g.67521055C>G

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