SNP Links for Gene (Select 101927549) - SNP

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Select item 14915512761.

rs1491551276 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TTT [Show Flanks]
Chromosome:: 10:105729256 (GRCh38)
10:107489015 (GRCh37)
Canonical SPDI:: NC_000010.11:105729256:TT:TTTTT
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTT=0.000224/1 (ALFA)
TTT=0.000019/2 (GnomAD)
TTT=0.000223/1 (Estonian)
HGVS:: NC_000010.11:g.105729258_105729259insTTT, NC_000010.10:g.107489016_107489017insTTT

Select item 14915270332.

rs1491527033 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:105729283 (GRCh38)
10:107489041 (GRCh37)
Canonical SPDI:: NC_000010.11:105729281:TAT:T
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000010.11:g.105729283_105729284del, NC_000010.10:g.107489041_107489042del

Select item 14915256123.

rs1491525612 has merged into rs11424054 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT [Show Flanks]
Chromosome:: 10:105810751 (GRCh38)
10:107570509 (GRCh37)
Canonical SPDI:: NC_000010.11:105810742:TTTTTTTTTTT:TTTTTTTT,NC_000010.11:105810742:TTTTTTTTTTT:TTTTTTTTT,NC_000010.11:105810742:TTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:105810742:TTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:105810742:TTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:105810742:TTTTTTTTTTT:TTTTTTTTTTTTTT
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
-=0.08643/207 (1000Genomes)
-=0.40218/1550 (ALSPAC)
-=0.412352/1529 (TWINSUK)
-=0.475/19 (GENOME_DK)
-=0.497034/131560 (TOPMED)
HGVS:: NC_000010.11:g.105810751_105810753del, NC_000010.11:g.105810752_105810753del, NC_000010.11:g.105810753del, NC_000010.11:g.105810753dup, NC_000010.11:g.105810752_105810753dup, NC_000010.11:g.105810751_105810753dup, NC_000010.10:g.107570509_107570511del, NC_000010.10:g.107570510_107570511del, NC_000010.10:g.107570511del, NC_000010.10:g.107570511dup, NC_000010.10:g.107570510_107570511dup, NC_000010.10:g.107570509_107570511dup

Select item 14914672274.

rs1491467227 [Homo sapiens]

Variant type:: INS
Alleles:: ->T,TA,TGTA,TGTGTGTA [Show Flanks]
Chromosome:: 10:105719887 (GRCh38)
10:107479646 (GRCh37)
Canonical SPDI:: NC_000010.11:105719887::T,NC_000010.11:105719887::TA,NC_000010.11:105719887::TGTA,NC_000010.11:105719887::TGTGTGTA
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTA=0./0 (ALFA)
T=0.00025/4 (TOMMO)
HGVS:: NC_000010.11:g.105719887_105719888insT, NC_000010.11:g.105719887_105719888insTA, NC_000010.11:g.105719887_105719888insTGTA, NC_000010.11:g.105719887_105719888insTGTGTGTA, NC_000010.10:g.107479645_107479646insT, NC_000010.10:g.107479645_107479646insTA, NC_000010.10:g.107479645_107479646insTGTA, NC_000010.10:g.107479645_107479646insTGTGTGTA

Select item 14914623485.

rs1491462348 [Homo sapiens]

Variant type:: INS
Alleles:: ->TA,TTA,TTTA [Show Flanks]
Chromosome:: 10:105729282 (GRCh38)
10:107489041 (GRCh37)
Canonical SPDI:: NC_000010.11:105729282::TA,NC_000010.11:105729282::TTA,NC_000010.11:105729282::TTTA
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTA=0./0 (ALFA)
TA=0.00002/2 (GnomAD)
HGVS:: NC_000010.11:g.105729282_105729283insTA, NC_000010.11:g.105729282_105729283insTTA, NC_000010.11:g.105729282_105729283insTTTA, NC_000010.10:g.107489040_107489041insTA, NC_000010.10:g.107489040_107489041insTTA, NC_000010.10:g.107489040_107489041insTTTA

Select item 14913858366.

rs1491385836 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TACATGTATGTATGTATATACACACA [Show Flanks]
Chromosome:: 10:105801482 (GRCh38)
10:107561241 (GRCh37)
Canonical SPDI:: NC_000010.11:105801482:ACACACATACATGTATGTATGTATATACACACA:ACACACATACATGTATGTATGTATATACACACATACATGTATGTATGTATATACACACA
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: ACACACATACATGTATGTATGTATATACACACATACATGTATGTATGTATATACACACA=0./0 (ALFA)
ACACACATACATGTATGTATGTATAT=0.000195/24 (GnomAD)
HGVS:: NC_000010.11:g.105801490_105801515dup, NC_000010.10:g.107561248_107561273dup

Select item 14913001967.

rs1491300196 has merged into rs757156774 [Homo sapiens]

Variant type:: DELINS
Alleles:: CACA>-,CA [Show Flanks]
Chromosome:: 10:105801486 (GRCh38)
10:107561244 (GRCh37)
Canonical SPDI:: NC_000010.11:105801481:CACACACA:CACA,NC_000010.11:105801481:CACACACA:CACACA
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACA=0.000084/1 (ALFA)
-=0.000008/1 (GnomAD)
HGVS:: NC_000010.11:g.105801482CA[2], NC_000010.11:g.105801482CA[3], NC_000010.10:g.107561240CA[2], NC_000010.10:g.107561240CA[3]

Select item 14912896098.

rs1491289609 has merged into rs34656890 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,TTTT,TTTTTT,TTTTTTATCCCCTATCTCTCTTTCTTTCTTTGAAAGTTTTTTTTCCTTTTTTTATCATTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:105804886 (GRCh38)
10:107564644 (GRCh37)
Canonical SPDI:: NC_000010.11:105804878:TTTTTTTTTTTT:TTTTTTT,NC_000010.11:105804878:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:105804878:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:105804878:TTTTTTTTTTTT:TTTTTTTTTTTTTATCCCCTATCTCTCTTTCTTTCTTTGAAAGTTTTTTTTCCTTTTTTTATCATTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.05/2 (GENOME_DK)
HGVS:: NC_000010.11:g.105804886_105804890del, NC_000010.11:g.105804890del, NC_000010.11:g.105804890dup, NC_000010.11:g.105804879_105804890T[13]ATCCCCTATCTCTCTTTCTTTCTTTGAAAGTTTTTTTTCCTTTTTTTATCATTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.10:g.107564644_107564648del, NC_000010.10:g.107564648del, NC_000010.10:g.107564648dup, NC_000010.10:g.107564637_107564648T[13]ATCCCCTATCTCTCTTTCTTTCTTTGAAAGTTTTTTTTCCTTTTTTTATCATTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14912516899.

rs1491251689 [Homo sapiens]

Variant type:: SNV:
Alleles:: AT>-
Chromosome:: no mapping
Canonical SPDI:

Select item 149112857610.

rs1491128576 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTGTGTGTGTTT,GTGTGTTT,GTGTTT,GTTT [Show Flanks]
Chromosome:: 10:105794344 (GRCh38)
10:107554103 (GRCh37)
Canonical SPDI:: NC_000010.11:105794344:T:TGTGTGTGTGTTT,NC_000010.11:105794344:T:TGTGTGTTT,NC_000010.11:105794344:T:TGTGTTT,NC_000010.11:105794344:T:TGTTT
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TGTGTGTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.105794345TG[5]TTT[1], NC_000010.11:g.105794345TG[3]TTT[1], NC_000010.11:g.105794345TG[2]TTT[1], NC_000010.11:g.105794345_105794346insGTTT, NC_000010.10:g.107554103TG[5]TTT[1], NC_000010.10:g.107554103TG[3]TTT[1], NC_000010.10:g.107554103TG[2]TTT[1], NC_000010.10:g.107554103_107554104insGTTT

Select item 149108291711.

rs1491082917 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 10:105701334 (GRCh38)
10:107461092 (GRCh37)
Canonical SPDI:: NC_000010.11:105701332:TCT:T
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000169/2 (ALFA)
-=0.000197/27 (GnomAD)
HGVS:: NC_000010.11:g.105701334_105701335del, NC_000010.10:g.107461092_107461093del

Select item 149108105012.

rs1491081050 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GA [Show Flanks]
Chromosome:: 10:105761183 (GRCh38)
10:107520942 (GRCh37)
Canonical SPDI:: NC_000010.11:105761183:GA:GAGA
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GAGA=0.000169/2 (ALFA)
GA=0.000025/3 (GnomAD)
HGVS:: NC_000010.11:g.105761184_105761185dup, NC_000010.10:g.107520942_107520943dup

Select item 149107522813.

rs1491075228 has merged into rs5787604 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAA>-,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:105717577 (GRCh38)
10:107477335 (GRCh37)
Canonical SPDI:: NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:105717564:AAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAA=0./0 (ALFA)
-=0.000091/24 (TOPMED)
-=0.043454/79 (Korea1K)
HGVS:: NC_000010.11:g.105717577_105717590del, NC_000010.11:g.105717581_105717590del, NC_000010.11:g.105717582_105717590del, NC_000010.11:g.105717583_105717590del, NC_000010.11:g.105717584_105717590del, NC_000010.11:g.105717588_105717590del, NC_000010.11:g.105717589_105717590del, NC_000010.11:g.105717590del, NC_000010.11:g.105717590dup, NC_000010.11:g.105717589_105717590dup, NC_000010.11:g.105717588_105717590dup, NC_000010.11:g.105717587_105717590dup, NC_000010.11:g.105717586_105717590dup, NC_000010.11:g.105717585_105717590dup, NC_000010.11:g.105717583_105717590dup, NC_000010.10:g.107477335_107477348del, NC_000010.10:g.107477339_107477348del, NC_000010.10:g.107477340_107477348del, NC_000010.10:g.107477341_107477348del, NC_000010.10:g.107477342_107477348del, NC_000010.10:g.107477346_107477348del, NC_000010.10:g.107477347_107477348del, NC_000010.10:g.107477348del, NC_000010.10:g.107477348dup, NC_000010.10:g.107477347_107477348dup, NC_000010.10:g.107477346_107477348dup, NC_000010.10:g.107477345_107477348dup, NC_000010.10:g.107477344_107477348dup, NC_000010.10:g.107477343_107477348dup, NC_000010.10:g.107477341_107477348dup

Select item 149106924214.

rs1491069242 [Homo sapiens]

Variant type:: DELINS
Alleles:: AG>- [Show Flanks]
Chromosome:: 10:105795512 (GRCh38)
10:107555270 (GRCh37)
Canonical SPDI:: NC_000010.11:105795507:AGAGAG:AGAG
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGAG=0.000071/1 (ALFA)
-=0.000029/4 (GnomAD)
-=0.000038/10 (TOPMED)
HGVS:: NC_000010.11:g.105795508AG[2], NC_000010.10:g.107555266AG[2]

Select item 149106217815.

rs1491062178 has merged into rs374216156 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:105701324 (GRCh38)
10:107461082 (GRCh37)
Canonical SPDI:: NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:105701318:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTT=0./0 (ALFA)
-=0.2734/1369 (1000Genomes)
HGVS:: NC_000010.11:g.105701324_105701333del, NC_000010.11:g.105701326_105701333del, NC_000010.11:g.105701327_105701333del, NC_000010.11:g.105701328_105701333del, NC_000010.11:g.105701329_105701333del, NC_000010.11:g.105701330_105701333del, NC_000010.11:g.105701332_105701333del, NC_000010.11:g.105701333del, NC_000010.11:g.105701333dup, NC_000010.11:g.105701332_105701333dup, NC_000010.11:g.105701331_105701333dup, NC_000010.11:g.105701330_105701333dup, NC_000010.11:g.105701329_105701333dup, NC_000010.11:g.105701328_105701333dup, NC_000010.11:g.105701327_105701333dup, NC_000010.11:g.105701326_105701333dup, NC_000010.11:g.105701325_105701333dup, NC_000010.11:g.105701324_105701333dup, NC_000010.11:g.105701319_105701333T[25]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.11:g.105701323_105701333dup, NC_000010.11:g.105701322_105701333dup, NC_000010.11:g.105701321_105701333dup, NC_000010.11:g.105701320_105701333dup, NC_000010.11:g.105701319_105701333dup, NC_000010.11:g.105701333_105701334insTTTTTTTTTTTTTTTT, NC_000010.11:g.105701333_105701334insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.105701333_105701334insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.107461082_107461091del, NC_000010.10:g.107461084_107461091del, NC_000010.10:g.107461085_107461091del, NC_000010.10:g.107461086_107461091del, NC_000010.10:g.107461087_107461091del, NC_000010.10:g.107461088_107461091del, NC_000010.10:g.107461090_107461091del, NC_000010.10:g.107461091del, NC_000010.10:g.107461091dup, NC_000010.10:g.107461090_107461091dup, NC_000010.10:g.107461089_107461091dup, NC_000010.10:g.107461088_107461091dup, NC_000010.10:g.107461087_107461091dup, NC_000010.10:g.107461086_107461091dup, NC_000010.10:g.107461085_107461091dup, NC_000010.10:g.107461084_107461091dup, NC_000010.10:g.107461083_107461091dup, NC_000010.10:g.107461082_107461091dup, NC_000010.10:g.107461077_107461091T[25]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.10:g.107461081_107461091dup, NC_000010.10:g.107461080_107461091dup, NC_000010.10:g.107461079_107461091dup, NC_000010.10:g.107461078_107461091dup, NC_000010.10:g.107461077_107461091dup, NC_000010.10:g.107461091_107461092insTTTTTTTTTTTTTTTT, NC_000010.10:g.107461091_107461092insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.107461091_107461092insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149104224316.

rs1491042243 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 10:105701318 (GRCh38)
10:107461076 (GRCh37)
Canonical SPDI:: NC_000010.11:105701316:TCT:T
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.00002/1 (GnomAD)
HGVS:: NC_000010.11:g.105701318_105701319del, NC_000010.10:g.107461076_107461077del

Select item 149102323717.

rs1491023237 has merged into rs768182981 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>- [Show Flanks]
Chromosome:: 10:105716671 (GRCh38)
10:107476429 (GRCh37)
Canonical SPDI:: NC_000010.11:105716669:TTT:T
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000023/3 (GnomAD)
HGVS:: NC_000010.11:g.105716671_105716672del, NC_000010.10:g.107476429_107476430del

Select item 149100670618.

rs1491006706 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TGGG [Show Flanks]
Chromosome:: 10:105753363 (GRCh38)
10:107513122 (GRCh37)
Canonical SPDI:: NC_000010.11:105753363:G:GTGGG
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTGGG=0./0 (ALFA)
GTGG=0.000004/1 (TOPMED)
GTGG=0.000008/1 (GnomAD)
HGVS:: NC_000010.11:g.105753364_105753365insTGGG, NC_000010.10:g.107513122_107513123insTGGG

Select item 149100004819.

rs1491000048 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:105724716 (GRCh38)
10:107484474 (GRCh37)
Canonical SPDI:: NC_000010.11:105724715:A:C
Gene:: LINC02627 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.105724716A>C, NC_000010.10:g.107484474A>C

Select item 149099425220.

rs1490994252 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:105681426 (GRCh38)
10:107441184 (GRCh37)
Canonical SPDI:: NC_000010.11:105681425:T:C
Gene:: LINC02627 (Varview), LOC107984266 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.105681426T>C, NC_000010.10:g.107441184T>C, XR_001747580.2:n.4403T>C

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