SNP Links for Gene (Select 389421) - SNP

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Select item 14915721531.

rs1491572153 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 6:105070641 (GRCh38)
6:105518516 (GRCh37)
Canonical SPDI:: NC_000006.12:105070640:CT:
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000006.12:g.105070641_105070642del, NC_000006.11:g.105518516_105518517del, NG_032815.1:g.118594_118595del

Select item 14915622282.

rs1491562228 [Homo sapiens]

Variant type:: DEL
Alleles:: AA>- [Show Flanks]
Chromosome:: 6:105023648 (GRCh38)
6:105471523 (GRCh37)
Canonical SPDI:: NC_000006.12:105023647:AA:
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00093/11 (ALFA)
-=0.00007/6 (GnomAD)
HGVS:: NC_000006.12:g.105023648_105023649del, NC_000006.11:g.105471523_105471524del, NG_032815.1:g.71601_71602del

Select item 14915620903.

rs1491562090 has merged into rs1185838727 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT [Show Flanks]
Chromosome:: 6:105023628 (GRCh38)
6:105471503 (GRCh37)
Canonical SPDI:: NC_000006.12:105023626:TTTT:T,NC_000006.12:105023626:TTTT:TT,NC_000006.12:105023626:TTTT:TTT
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.105023628_105023630del, NC_000006.12:g.105023629_105023630del, NC_000006.12:g.105023630del, NC_000006.11:g.105471503_105471505del, NC_000006.11:g.105471504_105471505del, NC_000006.11:g.105471505del, NG_032815.1:g.71581_71583del, NG_032815.1:g.71582_71583del, NG_032815.1:g.71583del

Select item 14915432834.

rs1491543283 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,TTT [Show Flanks]
Chromosome:: 6:105023665 (GRCh38)
6:105471540 (GRCh37)
Canonical SPDI:: NC_000006.12:105023659:TTTTTTT:TTTTT,NC_000006.12:105023659:TTTTTTT:TTTTTTTT
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTT=0./0 (ALFA)
-=0.00002/1 (GnomAD)
HGVS:: NC_000006.12:g.105023665_105023666del, NC_000006.12:g.105023666dup, NC_000006.11:g.105471540_105471541del, NC_000006.11:g.105471541dup, NG_032815.1:g.71618_71619del, NG_032815.1:g.71619dup

Select item 14915091605.

rs1491509160 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATAT>-,ATATAT [Show Flanks]
Chromosome:: 6:105023624 (GRCh38)
6:105471499 (GRCh37)
Canonical SPDI:: NC_000006.12:105023620:TATATAT:TAT,NC_000006.12:105023620:TATATAT:TATATATAT
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TATATATAT=0./0 (ALFA)
HGVS:: NC_000006.12:g.105023622AT[1], NC_000006.12:g.105023622AT[4], NC_000006.11:g.105471497AT[1], NC_000006.11:g.105471497AT[4], NG_032815.1:g.71575AT[1], NG_032815.1:g.71575AT[4]

Select item 14914979996.

rs1491497999 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 6:105023620 (GRCh38)
6:105471495 (GRCh37)
Canonical SPDI:: NC_000006.12:105023619:TT:
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.0007/12 (TOMMO)
HGVS:: NC_000006.12:g.105023620_105023621del, NC_000006.11:g.105471495_105471496del, NG_032815.1:g.71573_71574del

Select item 14914818327.

rs1491481832 has merged into rs1339964225 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATA>-,TA,TATATA [Show Flanks]
Chromosome:: 6:105023328 (GRCh38)
6:105471203 (GRCh37)
Canonical SPDI:: NC_000006.12:105023322:ATATATATA:ATATA,NC_000006.12:105023322:ATATATATA:ATATATA,NC_000006.12:105023322:ATATATATA:ATATATATATA
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATATATA=0./0 (ALFA)
-=0.00004/1 (TOMMO)
HGVS:: NC_000006.12:g.105023324TA[2], NC_000006.12:g.105023324TA[3], NC_000006.12:g.105023324TA[5], NC_000006.11:g.105471199TA[2], NC_000006.11:g.105471199TA[3], NC_000006.11:g.105471199TA[5], NG_032815.1:g.71277TA[2], NG_032815.1:g.71277TA[3], NG_032815.1:g.71277TA[5]

Select item 14914813728.

rs1491481372 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 6:105063649 (GRCh38)
6:105511525 (GRCh37)
Canonical SPDI:: NC_000006.12:105063649::G
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000006.12:g.105063649_105063650insG, NC_000006.11:g.105511524_105511525insG, NG_032815.1:g.111602_111603insG

Select item 14914024549.

rs1491402454 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 6:105023660 (GRCh38)
6:105471536 (GRCh37)
Canonical SPDI:: NC_000006.12:105023660::A
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.105023660_105023661insA, NC_000006.11:g.105471535_105471536insA, NG_032815.1:g.71613_71614insA

Select item 149138726010.

rs1491387260 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 6:105063636 (GRCh38)
6:105511512 (GRCh37)
Canonical SPDI:: NC_000006.12:105063636::C
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000006.12:g.105063636_105063637insC, NC_000006.11:g.105511511_105511512insC, NG_032815.1:g.111589_111590insC

Select item 149137678411.

rs1491376784 has merged into rs980799980 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 6:105030602 (GRCh38)
6:105478477 (GRCh37)
Canonical SPDI:: NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000006.12:105030592:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000006.12:g.105030602_105030613del, NC_000006.12:g.105030603_105030613del, NC_000006.12:g.105030604_105030613del, NC_000006.12:g.105030605_105030613del, NC_000006.12:g.105030607_105030613del, NC_000006.12:g.105030608_105030613del, NC_000006.12:g.105030609_105030613del, NC_000006.12:g.105030610_105030613del, NC_000006.12:g.105030611_105030613del, NC_000006.12:g.105030612_105030613del, NC_000006.12:g.105030613del, NC_000006.12:g.105030613dup, NC_000006.12:g.105030612_105030613dup, NC_000006.12:g.105030611_105030613dup, NC_000006.12:g.105030610_105030613dup, NC_000006.12:g.105030609_105030613dup, NC_000006.12:g.105030608_105030613dup, NC_000006.12:g.105030607_105030613dup, NC_000006.12:g.105030606_105030613dup, NC_000006.12:g.105030605_105030613dup, NC_000006.12:g.105030604_105030613dup, NC_000006.12:g.105030603_105030613dup, NC_000006.12:g.105030602_105030613dup, NC_000006.12:g.105030601_105030613dup, NC_000006.12:g.105030600_105030613dup, NC_000006.12:g.105030599_105030613dup, NC_000006.12:g.105030597_105030613dup, NC_000006.12:g.105030593_105030613dup, NC_000006.11:g.105478477_105478488del, NC_000006.11:g.105478478_105478488del, NC_000006.11:g.105478479_105478488del, NC_000006.11:g.105478480_105478488del, NC_000006.11:g.105478482_105478488del, NC_000006.11:g.105478483_105478488del, NC_000006.11:g.105478484_105478488del, NC_000006.11:g.105478485_105478488del, NC_000006.11:g.105478486_105478488del, NC_000006.11:g.105478487_105478488del, NC_000006.11:g.105478488del, NC_000006.11:g.105478488dup, NC_000006.11:g.105478487_105478488dup, NC_000006.11:g.105478486_105478488dup, NC_000006.11:g.105478485_105478488dup, NC_000006.11:g.105478484_105478488dup, NC_000006.11:g.105478483_105478488dup, NC_000006.11:g.105478482_105478488dup, NC_000006.11:g.105478481_105478488dup, NC_000006.11:g.105478480_105478488dup, NC_000006.11:g.105478479_105478488dup, NC_000006.11:g.105478478_105478488dup, NC_000006.11:g.105478477_105478488dup, NC_000006.11:g.105478476_105478488dup, NC_000006.11:g.105478475_105478488dup, NC_000006.11:g.105478474_105478488dup, NC_000006.11:g.105478472_105478488dup, NC_000006.11:g.105478468_105478488dup, NG_032815.1:g.78555_78566del, NG_032815.1:g.78556_78566del, NG_032815.1:g.78557_78566del, NG_032815.1:g.78558_78566del, NG_032815.1:g.78560_78566del, NG_032815.1:g.78561_78566del, NG_032815.1:g.78562_78566del, NG_032815.1:g.78563_78566del, NG_032815.1:g.78564_78566del, NG_032815.1:g.78565_78566del, NG_032815.1:g.78566del, NG_032815.1:g.78566dup, NG_032815.1:g.78565_78566dup, NG_032815.1:g.78564_78566dup, NG_032815.1:g.78563_78566dup, NG_032815.1:g.78562_78566dup, NG_032815.1:g.78561_78566dup, NG_032815.1:g.78560_78566dup, NG_032815.1:g.78559_78566dup, NG_032815.1:g.78558_78566dup, NG_032815.1:g.78557_78566dup, NG_032815.1:g.78556_78566dup, NG_032815.1:g.78555_78566dup, NG_032815.1:g.78554_78566dup, NG_032815.1:g.78553_78566dup, NG_032815.1:g.78552_78566dup, NG_032815.1:g.78550_78566dup, NG_032815.1:g.78546_78566dup

Select item 149136913912.

rs1491369139 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CTT [Show Flanks]
Chromosome:: 6:105030593 (GRCh38)
6:105478469 (GRCh37)
Canonical SPDI:: NC_000006.12:105030593:TT:TTCTT
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TTCTT=0./0 (ALFA)
HGVS:: NC_000006.12:g.105030595_105030596insCTT, NC_000006.11:g.105478470_105478471insCTT, NG_032815.1:g.78548_78549insCTT

Select item 149136709213.

rs1491367092 has merged into rs762449779 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGGGG>-,G,GG,GGG,GGGG,GGGGGG,GGGGGGG,GGGGGGGG [Show Flanks]
Chromosome:: 6:105063644 (GRCh38)
6:105511519 (GRCh37)
Canonical SPDI:: NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGG,NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGGG,NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGGGG,NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGGGGG,NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGGGGGG,NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGGGGGGGG,NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGGGGGGGGG,NC_000006.12:105063635:GGGGGGGGGGGGG:GGGGGGGGGGGGGGGG
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGGGGGGGGGG=0./0 (ALFA)
-=0.06227/240 (ALSPAC)
HGVS:: NC_000006.12:g.105063644_105063648del, NC_000006.12:g.105063645_105063648del, NC_000006.12:g.105063646_105063648del, NC_000006.12:g.105063647_105063648del, NC_000006.12:g.105063648del, NC_000006.12:g.105063648dup, NC_000006.12:g.105063647_105063648dup, NC_000006.12:g.105063646_105063648dup, NC_000006.11:g.105511519_105511523del, NC_000006.11:g.105511520_105511523del, NC_000006.11:g.105511521_105511523del, NC_000006.11:g.105511522_105511523del, NC_000006.11:g.105511523del, NC_000006.11:g.105511523dup, NC_000006.11:g.105511522_105511523dup, NC_000006.11:g.105511521_105511523dup, NG_032815.1:g.111597_111601del, NG_032815.1:g.111598_111601del, NG_032815.1:g.111599_111601del, NG_032815.1:g.111600_111601del, NG_032815.1:g.111601del, NG_032815.1:g.111601dup, NG_032815.1:g.111600_111601dup, NG_032815.1:g.111599_111601dup

Select item 149135926114.

rs1491359261 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 6:104935005 (GRCh38)
6:105382881 (GRCh37)
Canonical SPDI:: NC_000006.12:104935005:TTTTTT:TTTTTTT
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
T=0.000076/20 (TOPMED)
T=0.000079/11 (GnomAD)
HGVS:: NC_000006.12:g.104935011dup, NC_000006.11:g.105382886dup

Select item 149133537015.

rs1491335370 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 6:104935005 (GRCh38)
6:105382880 (GRCh37)
Canonical SPDI:: NC_000006.12:104935004:CT:
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.104935005_104935006del, NC_000006.11:g.105382880_105382881del

Select item 149133028816.

rs1491330288 [Homo sapiens]

Variant type:: INS
Alleles:: ->G,GTG [Show Flanks]
Chromosome:: 6:104992515 (GRCh38)
6:105440391 (GRCh37)
Canonical SPDI:: NC_000006.12:104992515::G,NC_000006.12:104992515::GTG
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GTG=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.028947/469 (TOMMO)
HGVS:: NC_000006.12:g.104992515_104992516insG, NC_000006.12:g.104992515_104992516insGTG, NC_000006.11:g.105440390_105440391insG, NC_000006.11:g.105440390_105440391insGTG, NG_032815.1:g.40468_40469insG, NG_032815.1:g.40468_40469insGTG

Select item 149132706017.

rs1491327060 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TAT [Show Flanks]
Chromosome:: 6:105023323 (GRCh38)
6:105471199 (GRCh37)
Canonical SPDI:: NC_000006.12:105023323:TAT:TATTAT
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TATTAT=0.00042/5 (ALFA)
HGVS:: NC_000006.12:g.105023324_105023326dup, NC_000006.11:g.105471199_105471201dup, NG_032815.1:g.71277_71279dup

Select item 149130197318.

rs1491301973 has merged into rs1230150037 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA [Show Flanks]
Chromosome:: 6:105063651 (GRCh38)
6:105511526 (GRCh37)
Canonical SPDI:: NC_000006.12:105063648:AAAAAAA:AA,NC_000006.12:105063648:AAAAAAA:AAA,NC_000006.12:105063648:AAAAAAA:AAAA,NC_000006.12:105063648:AAAAAAA:AAAAA,NC_000006.12:105063648:AAAAAAA:AAAAAA,NC_000006.12:105063648:AAAAAAA:AAAAAAAA,NC_000006.12:105063648:AAAAAAA:AAAAAAAAA,NC_000006.12:105063648:AAAAAAA:AAAAAAAAAA,NC_000006.12:105063648:AAAAAAA:AAAAAAAAAAA
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AA=0./0 (ALFA)
HGVS:: NC_000006.12:g.105063651_105063655del, NC_000006.12:g.105063652_105063655del, NC_000006.12:g.105063653_105063655del, NC_000006.12:g.105063654_105063655del, NC_000006.12:g.105063655del, NC_000006.12:g.105063655dup, NC_000006.12:g.105063654_105063655dup, NC_000006.12:g.105063653_105063655dup, NC_000006.12:g.105063652_105063655dup, NC_000006.11:g.105511526_105511530del, NC_000006.11:g.105511527_105511530del, NC_000006.11:g.105511528_105511530del, NC_000006.11:g.105511529_105511530del, NC_000006.11:g.105511530del, NC_000006.11:g.105511530dup, NC_000006.11:g.105511529_105511530dup, NC_000006.11:g.105511528_105511530dup, NC_000006.11:g.105511527_105511530dup, NG_032815.1:g.111604_111608del, NG_032815.1:g.111605_111608del, NG_032815.1:g.111606_111608del, NG_032815.1:g.111607_111608del, NG_032815.1:g.111608del, NG_032815.1:g.111608dup, NG_032815.1:g.111607_111608dup, NG_032815.1:g.111606_111608dup, NG_032815.1:g.111605_111608dup

Select item 149130026619.

rs1491300266 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 6:105017072 (GRCh38)
6:105464947 (GRCh37)
Canonical SPDI:: NC_000006.12:105017071:CA:
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00017/2 (ALFA)
HGVS:: NC_000006.12:g.105017072_105017073del, NC_000006.11:g.105464947_105464948del, NG_032815.1:g.65025_65026del

Select item 149129238320.

rs1491292383 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 6:105023584 (GRCh38)
6:105471459 (GRCh37)
Canonical SPDI:: NC_000006.12:105023583:TT:
Gene:: LIN28B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00143/17 (ALFA)
-=0.00012/2 (TOMMO)
HGVS:: NC_000006.12:g.105023584_105023585del, NC_000006.11:g.105471459_105471460del, NG_032815.1:g.71537_71538del

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