SNP Links for Gene (Select 163747) - SNP

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Select item 14915832051.

rs1491583205 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 1:54825041 (GRCh38)
1:55290714 (GRCh37)
Canonical SPDI:: NC_000001.11:54825040:CT:
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant,downstream_transcript_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.00041/11 (TOMMO)
HGVS:: NC_000001.11:g.54825041_54825042del, NC_000001.10:g.55290714_55290715del

Select item 14913810062.

rs1491381006 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TT [Show Flanks]
Chromosome:: 1:54819928 (GRCh38)
1:55285602 (GRCh37)
Canonical SPDI:: NC_000001.11:54819928:T:TTT
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by cluster
HGVS:: NC_000001.11:g.54819929_54819930insTT, NC_000001.10:g.55285602_55285603insTT

Select item 14913321153.

rs1491332115 has merged into rs1553190225 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTCT>-,CT,CTCTCT,CTCTCTCT [Show Flanks]
Chromosome:: 1:54820112 (GRCh38)
1:55285785 (GRCh37)
Canonical SPDI:: NC_000001.11:54820102:TCTCTCTCTCTCT:TCTCTCTCT,NC_000001.11:54820102:TCTCTCTCTCTCT:TCTCTCTCTCT,NC_000001.11:54820102:TCTCTCTCTCTCT:TCTCTCTCTCTCTCT,NC_000001.11:54820102:TCTCTCTCTCTCT:TCTCTCTCTCTCTCTCT
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TCTCTCTCTCT=0./0 (ALFA)
-=0.00012/2 (GnomAD)
HGVS:: NC_000001.11:g.54820104CT[4], NC_000001.11:g.54820104CT[5], NC_000001.11:g.54820104CT[7], NC_000001.11:g.54820104CT[8], NC_000001.10:g.55285777CT[4], NC_000001.10:g.55285777CT[5], NC_000001.10:g.55285777CT[7], NC_000001.10:g.55285777CT[8]

Select item 14913113614.

rs1491311361 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GCGGG,GGCGGG,GGG,GGGG,GGGGG,GGGGGG,GGGGGGG,GGGGGGGG,GGGGGGGGG [Show Flanks]
Chromosome:: 1:54808618 (GRCh38)
1:55274292 (GRCh37)
Canonical SPDI:: NC_000001.11:54808618:GGG:GGGGCGGG,NC_000001.11:54808618:GGG:GGGGGCGGG,NC_000001.11:54808618:GGG:GGGGGG,NC_000001.11:54808618:GGG:GGGGGGG,NC_000001.11:54808618:GGG:GGGGGGGG,NC_000001.11:54808618:GGG:GGGGGGGGG,NC_000001.11:54808618:GGG:GGGGGGGGGG,NC_000001.11:54808618:GGG:GGGGGGGGGGG,NC_000001.11:54808618:GGG:GGGGGGGGGGGG
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGCGGG=0./0 (ALFA)
HGVS:: NC_000001.11:g.54808619_54808621G[4]CGGG[1], NC_000001.11:g.54808619_54808621G[5]CGGG[1], NC_000001.11:g.54808619_54808621dup, NC_000001.11:g.54808621_54808622insGGGG, NC_000001.11:g.54808621_54808622insGGGGG, NC_000001.11:g.54808621_54808622insGGGGGG, NC_000001.11:g.54808621_54808622insGGGGGGG, NC_000001.11:g.54808621_54808622insGGGGGGGG, NC_000001.11:g.54808621_54808622insGGGGGGGGG, NC_000001.10:g.55274292_55274294G[4]CGGG[1], NC_000001.10:g.55274292_55274294G[5]CGGG[1], NC_000001.10:g.55274292_55274294dup, NC_000001.10:g.55274294_55274295insGGGG, NC_000001.10:g.55274294_55274295insGGGGG, NC_000001.10:g.55274294_55274295insGGGGGG, NC_000001.10:g.55274294_55274295insGGGGGGG, NC_000001.10:g.55274294_55274295insGGGGGGGG, NC_000001.10:g.55274294_55274295insGGGGGGGGG

Select item 14911819675.

rs1491181967 has merged into rs55722007 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:54825052 (GRCh38)
1:55290725 (GRCh37)
Canonical SPDI:: NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54825041:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
TTTTTTTTTTTTTTT=0./0 (GENOME_DK)
HGVS:: NC_000001.11:g.54825052_54825067del, NC_000001.11:g.54825053_54825067del, NC_000001.11:g.54825054_54825067del, NC_000001.11:g.54825055_54825067del, NC_000001.11:g.54825056_54825067del, NC_000001.11:g.54825057_54825067del, NC_000001.11:g.54825058_54825067del, NC_000001.11:g.54825059_54825067del, NC_000001.11:g.54825060_54825067del, NC_000001.11:g.54825061_54825067del, NC_000001.11:g.54825062_54825067del, NC_000001.11:g.54825063_54825067del, NC_000001.11:g.54825064_54825067del, NC_000001.11:g.54825065_54825067del, NC_000001.11:g.54825066_54825067del, NC_000001.11:g.54825067del, NC_000001.11:g.54825067dup, NC_000001.11:g.54825066_54825067dup, NC_000001.11:g.54825060_54825067dup, NC_000001.10:g.55290725_55290740del, NC_000001.10:g.55290726_55290740del, NC_000001.10:g.55290727_55290740del, NC_000001.10:g.55290728_55290740del, NC_000001.10:g.55290729_55290740del, NC_000001.10:g.55290730_55290740del, NC_000001.10:g.55290731_55290740del, NC_000001.10:g.55290732_55290740del, NC_000001.10:g.55290733_55290740del, NC_000001.10:g.55290734_55290740del, NC_000001.10:g.55290735_55290740del, NC_000001.10:g.55290736_55290740del, NC_000001.10:g.55290737_55290740del, NC_000001.10:g.55290738_55290740del, NC_000001.10:g.55290739_55290740del, NC_000001.10:g.55290740del, NC_000001.10:g.55290740dup, NC_000001.10:g.55290739_55290740dup, NC_000001.10:g.55290733_55290740dup

Select item 14911718826.

rs1491171882 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 1:54820115 (GRCh38)
1:55285789 (GRCh37)
Canonical SPDI:: NC_000001.11:54820115::C
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.0017/11 (GnomAD)
HGVS:: NC_000001.11:g.54820115_54820116insC, NC_000001.10:g.55285788_55285789insC

Select item 14911170937.

rs1491117093 has merged into rs71740547 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 1:54808618 (GRCh38)
1:55274291 (GRCh37)
Canonical SPDI:: NC_000001.11:54808616:GAG:G
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.045126/736 (ALFA)
-=0.06291/8182 (GnomAD)
-=0.085491/317 (TWINSUK)
-=0.087442/337 (ALSPAC)
-=0.101637/509 (1000Genomes)
-=0.162118/297 (Korea1K)
-=0.20081/3287 (TOMMO)
HGVS:: NC_000001.11:g.54808618_54808619del, NC_000001.10:g.55274291_55274292del

Select item 14909681928.

rs1490968192 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:54823152 (GRCh38)
1:55288825 (GRCh37)
Canonical SPDI:: NC_000001.11:54823151:A:G
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.54823152A>G, NC_000001.10:g.55288825A>G

Select item 14909435849.

rs1490943584 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:54822126 (GRCh38)
1:55287799 (GRCh37)
Canonical SPDI:: NC_000001.11:54822125:C:T
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.54822126C>T, NC_000001.10:g.55287799C>T

Select item 149092492810.

rs1490924928 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 1:54808324 (GRCh38)
1:55273997 (GRCh37)
Canonical SPDI:: NC_000001.11:54808323:A:
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.54808324del, NC_000001.10:g.55273997del

Select item 149078491611.

rs1490784916 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:54826728 (GRCh38)
1:55292401 (GRCh37)
Canonical SPDI:: NC_000001.11:54826727:T:C
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.54826728T>C, NC_000001.10:g.55292401T>C

Select item 149066555212.

rs1490665552 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:54814424 (GRCh38)
1:55280097 (GRCh37)
Canonical SPDI:: NC_000001.11:54814423:TG:
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.54814424_54814425del, NC_000001.10:g.55280097_55280098del

Select item 149049646813.

rs1490496468 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54809411 (GRCh38)
1:55275084 (GRCh37)
Canonical SPDI:: NC_000001.11:54809410:G:A
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.54809411G>A, NC_000001.10:g.55275084G>A

Select item 149043581714.

rs1490435817 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:54831802 (GRCh38)
1:55297475 (GRCh37)
Canonical SPDI:: NC_000001.11:54831801:T:C
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.54831802T>C, NC_000001.10:g.55297475T>C

Select item 149039272015.

rs1490392720 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:54811732 (GRCh38)
1:55277405 (GRCh37)
Canonical SPDI:: NC_000001.11:54811731:C:G,NC_000001.11:54811731:C:T
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.54811732C>G, NC_000001.11:g.54811732C>T, NC_000001.10:g.55277405C>G, NC_000001.10:g.55277405C>T

Select item 149025300316.

rs1490253003 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:54830013 (GRCh38)
1:55295686 (GRCh37)
Canonical SPDI:: NC_000001.11:54830012:G:A
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.54830013G>A, NC_000001.10:g.55295686G>A

Select item 149021107217.

rs1490211072 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:54833386 (GRCh38)
1:55299059 (GRCh37)
Canonical SPDI:: NC_000001.11:54833385:C:T
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.54833386C>T, NC_000001.10:g.55299059C>T

Select item 149013525318.

rs1490135253 has merged into rs1162228188 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 1:54821899 (GRCh38)
1:55287572 (GRCh37)
Canonical SPDI:: NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000001.11:54821886:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000001.11:g.54821899_54821916del, NC_000001.11:g.54821900_54821916del, NC_000001.11:g.54821901_54821916del, NC_000001.11:g.54821902_54821916del, NC_000001.11:g.54821903_54821916del, NC_000001.11:g.54821904_54821916del, NC_000001.11:g.54821905_54821916del, NC_000001.11:g.54821906_54821916del, NC_000001.11:g.54821907_54821916del, NC_000001.11:g.54821908_54821916del, NC_000001.11:g.54821909_54821916del, NC_000001.11:g.54821910_54821916del, NC_000001.11:g.54821911_54821916del, NC_000001.11:g.54821912_54821916del, NC_000001.11:g.54821913_54821916del, NC_000001.11:g.54821914_54821916del, NC_000001.11:g.54821915_54821916del, NC_000001.11:g.54821916del, NC_000001.11:g.54821916dup, NC_000001.11:g.54821915_54821916dup, NC_000001.11:g.54821914_54821916dup, NC_000001.11:g.54821913_54821916dup, NC_000001.11:g.54821912_54821916dup, NC_000001.11:g.54821911_54821916dup, NC_000001.11:g.54821910_54821916dup, NC_000001.11:g.54821909_54821916dup, NC_000001.11:g.54821908_54821916dup, NC_000001.11:g.54821907_54821916dup, NC_000001.11:g.54821906_54821916dup, NC_000001.11:g.54821905_54821916dup, NC_000001.11:g.54821903_54821916dup, NC_000001.11:g.54821901_54821916dup, NC_000001.11:g.54821889_54821916dup, NC_000001.10:g.55287572_55287589del, NC_000001.10:g.55287573_55287589del, NC_000001.10:g.55287574_55287589del, NC_000001.10:g.55287575_55287589del, NC_000001.10:g.55287576_55287589del, NC_000001.10:g.55287577_55287589del, NC_000001.10:g.55287578_55287589del, NC_000001.10:g.55287579_55287589del, NC_000001.10:g.55287580_55287589del, NC_000001.10:g.55287581_55287589del, NC_000001.10:g.55287582_55287589del, NC_000001.10:g.55287583_55287589del, NC_000001.10:g.55287584_55287589del, NC_000001.10:g.55287585_55287589del, NC_000001.10:g.55287586_55287589del, NC_000001.10:g.55287587_55287589del, NC_000001.10:g.55287588_55287589del, NC_000001.10:g.55287589del, NC_000001.10:g.55287589dup, NC_000001.10:g.55287588_55287589dup, NC_000001.10:g.55287587_55287589dup, NC_000001.10:g.55287586_55287589dup, NC_000001.10:g.55287585_55287589dup, NC_000001.10:g.55287584_55287589dup, NC_000001.10:g.55287583_55287589dup, NC_000001.10:g.55287582_55287589dup, NC_000001.10:g.55287581_55287589dup, NC_000001.10:g.55287580_55287589dup, NC_000001.10:g.55287579_55287589dup, NC_000001.10:g.55287578_55287589dup, NC_000001.10:g.55287576_55287589dup, NC_000001.10:g.55287574_55287589dup, NC_000001.10:g.55287562_55287589dup

Select item 149009036519.

rs1490090365 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:54815942 (GRCh38)
1:55281615 (GRCh37)
Canonical SPDI:: NC_000001.11:54815941:A:T
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000015/2 (GnomAD)
HGVS:: NC_000001.11:g.54815942A>T, NC_000001.10:g.55281615A>T

Select item 149006446120.

rs1490064461 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:54813596 (GRCh38)
1:55279269 (GRCh37)
Canonical SPDI:: NC_000001.11:54813595:A:G
Gene:: LEXM (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000001.11:g.54813596A>G, NC_000001.10:g.55279269A>G

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