SNP Links for Gene (Select 23185) - SNP

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Select item 14915280721.

rs1491528072 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 10:808725 (GRCh38)
10:854666 (GRCh37)
Canonical SPDI:: NC_000010.11:808725:T:TT
Gene:: LARP4B (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000185/49 (TOPMED)
T=0.000193/18 (GnomAD)
HGVS:: NC_000010.11:g.808726dup, NC_000010.10:g.854666dup, XM_017015990.2:c.*4200dup, XM_017015987.2:c.*4200dup, XM_017015988.2:c.*4200dup, NM_001351277.2:c.*4200dup, NM_001351277.1:c.*4200dup, NM_015155.2:c.*4200dup, XM_017015992.2:c.*4200dup, XM_047424892.1:c.*4200dup, XM_047424896.1:c.*4200dup, XM_047424893.1:c.*4200dup, XM_047424895.1:c.*4200dup, XM_047424894.1:c.*4200dup, XM_047424897.1:c.*4200dup, XM_047424902.1:c.*4200dup

Select item 14914655452.

rs1491465545 [Homo sapiens]

Variant type:: INS
Alleles:: ->C [Show Flanks]
Chromosome:: 10:902640 (GRCh38)
10:948581 (GRCh37)
Canonical SPDI:: NC_000010.11:902640::C
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000033/3 (GnomAD)
C=0.000049/13 (TOPMED)
HGVS:: NC_000010.11:g.902640_902641insC, NC_000010.10:g.948580_948581insC

Select item 14913897253.

rs1491389725 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATCCCTCTTGTTCACCA [Show Flanks]
Chromosome:: 10:924847 (GRCh38)
10:970788 (GRCh37)
Canonical SPDI:: NC_000010.11:924847:ATCCCTCTTGTTCACCA:ATCCCTCTTGTTCACCAATCCCTCTTGTTCACCA
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: ATCCCTCTTGTTCACCAATCCCTCTTGTTCACCA=0./0 (ALFA)
HGVS:: NC_000010.11:g.924848_924864dup, NC_000010.10:g.970788_970804dup, XM_047424892.1:c.-13225_-13209dup, XM_047424896.1:c.-13225_-13209dup, XM_047424899.1:c.-13225_-13209dup

Select item 14913281194.

rs1491328119 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CAA [Show Flanks]
Chromosome:: 10:888338 (GRCh38)
10:934279 (GRCh37)
Canonical SPDI:: NC_000010.11:888338:AA:AACAA
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
HGVS:: NC_000010.11:g.888340_888341insCAA, NC_000010.10:g.934280_934281insCAA

Select item 14912674815.

rs1491267481 [Homo sapiens]

Variant type:: DELINS
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:924848 (GRCh38)
10:970788 (GRCh37)
Canonical SPDI:: NC_000010.11:924846:TAT:T
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.924848_924849del, NC_000010.10:g.970788_970789del, XM_047424892.1:c.-13209_-13208del, XM_047424896.1:c.-13209_-13208del, XM_047424899.1:c.-13209_-13208del

Select item 14912537306.

rs1491253730 has merged into rs56051964 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:892917 (GRCh38)
10:938857 (GRCh37)
Canonical SPDI:: NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:892902:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LARP4B (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.892917_892927del, NC_000010.11:g.892918_892927del, NC_000010.11:g.892919_892927del, NC_000010.11:g.892920_892927del, NC_000010.11:g.892921_892927del, NC_000010.11:g.892922_892927del, NC_000010.11:g.892923_892927del, NC_000010.11:g.892924_892927del, NC_000010.11:g.892925_892927del, NC_000010.11:g.892926_892927del, NC_000010.11:g.892927del, NC_000010.11:g.892927dup, NC_000010.11:g.892926_892927dup, NC_000010.11:g.892925_892927dup, NC_000010.11:g.892924_892927dup, NC_000010.11:g.892906_892927dup, NC_000010.11:g.892927_892928insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.938857_938867del, NC_000010.10:g.938858_938867del, NC_000010.10:g.938859_938867del, NC_000010.10:g.938860_938867del, NC_000010.10:g.938861_938867del, NC_000010.10:g.938862_938867del, NC_000010.10:g.938863_938867del, NC_000010.10:g.938864_938867del, NC_000010.10:g.938865_938867del, NC_000010.10:g.938866_938867del, NC_000010.10:g.938867del, NC_000010.10:g.938867dup, NC_000010.10:g.938866_938867dup, NC_000010.10:g.938865_938867dup, NC_000010.10:g.938864_938867dup, NC_000010.10:g.938846_938867dup, NC_000010.10:g.938867_938868insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, XM_017015990.2:c.-2369_-2359del, XM_017015990.2:c.-2368_-2359del, XM_017015990.2:c.-2367_-2359del, XM_017015990.2:c.-2366_-2359del, XM_017015990.2:c.-2365_-2359del, XM_017015990.2:c.-2364_-2359del, XM_017015990.2:c.-2363_-2359del, XM_017015990.2:c.-2362_-2359del, XM_017015990.2:c.-2361_-2359del, XM_017015990.2:c.-2360_-2359del, XM_017015990.2:c.-2359del, XM_017015990.2:c.-2359dup, XM_017015990.2:c.-2360_-2359dup, XM_017015990.2:c.-2361_-2359dup, XM_017015990.2:c.-2362_-2359dup, XM_017015990.2:c.-2380_-2359dup, XM_017015990.2:c.-2359_-2358insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA

Select item 14912536207.

rs1491253620 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:918632 (GRCh38)
10:964572 (GRCh37)
Canonical SPDI:: NC_000010.11:918631:CA:
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.918632_918633del, NC_000010.10:g.964572_964573del, XM_047424892.1:c.-6994_-6993del, XM_047424896.1:c.-6994_-6993del, XM_047424899.1:c.-6994_-6993del

Select item 14912487188.

rs1491248718 has merged into rs57396015 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAA>-,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:918644 (GRCh38)
10:964584 (GRCh37)
Canonical SPDI:: NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:918632:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LARP4B (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.918644_918656del, NC_000010.11:g.918646_918656del, NC_000010.11:g.918647_918656del, NC_000010.11:g.918648_918656del, NC_000010.11:g.918649_918656del, NC_000010.11:g.918650_918656del, NC_000010.11:g.918651_918656del, NC_000010.11:g.918652_918656del, NC_000010.11:g.918653_918656del, NC_000010.11:g.918654_918656del, NC_000010.11:g.918655_918656del, NC_000010.11:g.918656del, NC_000010.11:g.918656dup, NC_000010.11:g.918655_918656dup, NC_000010.11:g.918654_918656dup, NC_000010.11:g.918653_918656dup, NC_000010.11:g.918652_918656dup, NC_000010.11:g.918651_918656dup, NC_000010.11:g.918650_918656dup, NC_000010.11:g.918649_918656dup, NC_000010.11:g.918648_918656dup, NC_000010.10:g.964584_964596del, NC_000010.10:g.964586_964596del, NC_000010.10:g.964587_964596del, NC_000010.10:g.964588_964596del, NC_000010.10:g.964589_964596del, NC_000010.10:g.964590_964596del, NC_000010.10:g.964591_964596del, NC_000010.10:g.964592_964596del, NC_000010.10:g.964593_964596del, NC_000010.10:g.964594_964596del, NC_000010.10:g.964595_964596del, NC_000010.10:g.964596del, NC_000010.10:g.964596dup, NC_000010.10:g.964595_964596dup, NC_000010.10:g.964594_964596dup, NC_000010.10:g.964593_964596dup, NC_000010.10:g.964592_964596dup, NC_000010.10:g.964591_964596dup, NC_000010.10:g.964590_964596dup, NC_000010.10:g.964589_964596dup, NC_000010.10:g.964588_964596dup, XM_047424892.1:c.-7006_-6994del, XM_047424892.1:c.-7004_-6994del, XM_047424892.1:c.-7003_-6994del, XM_047424892.1:c.-7002_-6994del, XM_047424892.1:c.-7001_-6994del, XM_047424892.1:c.-7000_-6994del, XM_047424892.1:c.-6999_-6994del, XM_047424892.1:c.-6998_-6994del, XM_047424892.1:c.-6997_-6994del, XM_047424892.1:c.-6996_-6994del, XM_047424892.1:c.-6995_-6994del, XM_047424892.1:c.-6994del, XM_047424892.1:c.-6994dup, XM_047424892.1:c.-6995_-6994dup, XM_047424892.1:c.-6996_-6994dup, XM_047424892.1:c.-6997_-6994dup, XM_047424892.1:c.-6998_-6994dup, XM_047424892.1:c.-6999_-6994dup, XM_047424892.1:c.-7000_-6994dup, XM_047424892.1:c.-7001_-6994dup, XM_047424892.1:c.-7002_-6994dup, XM_047424896.1:c.-7006_-6994del, XM_047424896.1:c.-7004_-6994del, XM_047424896.1:c.-7003_-6994del, XM_047424896.1:c.-7002_-6994del, XM_047424896.1:c.-7001_-6994del, XM_047424896.1:c.-7000_-6994del, XM_047424896.1:c.-6999_-6994del, XM_047424896.1:c.-6998_-6994del, XM_047424896.1:c.-6997_-6994del, XM_047424896.1:c.-6996_-6994del, XM_047424896.1:c.-6995_-6994del, XM_047424896.1:c.-6994del, XM_047424896.1:c.-6994dup, XM_047424896.1:c.-6995_-6994dup, XM_047424896.1:c.-6996_-6994dup, XM_047424896.1:c.-6997_-6994dup, XM_047424896.1:c.-6998_-6994dup, XM_047424896.1:c.-6999_-6994dup, XM_047424896.1:c.-7000_-6994dup, XM_047424896.1:c.-7001_-6994dup, XM_047424896.1:c.-7002_-6994dup, XM_047424899.1:c.-7006_-6994del, XM_047424899.1:c.-7004_-6994del, XM_047424899.1:c.-7003_-6994del, XM_047424899.1:c.-7002_-6994del, XM_047424899.1:c.-7001_-6994del, XM_047424899.1:c.-7000_-6994del, XM_047424899.1:c.-6999_-6994del, XM_047424899.1:c.-6998_-6994del, XM_047424899.1:c.-6997_-6994del, XM_047424899.1:c.-6996_-6994del, XM_047424899.1:c.-6995_-6994del, XM_047424899.1:c.-6994del, XM_047424899.1:c.-6994dup, XM_047424899.1:c.-6995_-6994dup, XM_047424899.1:c.-6996_-6994dup, XM_047424899.1:c.-6997_-6994dup, XM_047424899.1:c.-6998_-6994dup, XM_047424899.1:c.-6999_-6994dup, XM_047424899.1:c.-7000_-6994dup, XM_047424899.1:c.-7001_-6994dup, XM_047424899.1:c.-7002_-6994dup

Select item 14912342839.

rs1491234283 has merged into rs34586444 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTT>-,T,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:900928 (GRCh38)
10:946868 (GRCh37)
Canonical SPDI:: NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:900919:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LARP4B (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTT=0./0 (ALFA)
HGVS:: NC_000010.11:g.900928_900936del, NC_000010.11:g.900929_900936del, NC_000010.11:g.900931_900936del, NC_000010.11:g.900932_900936del, NC_000010.11:g.900933_900936del, NC_000010.11:g.900934_900936del, NC_000010.11:g.900935_900936del, NC_000010.11:g.900936del, NC_000010.11:g.900936dup, NC_000010.11:g.900935_900936dup, NC_000010.11:g.900934_900936dup, NC_000010.11:g.900933_900936dup, NC_000010.11:g.900932_900936dup, NC_000010.11:g.900931_900936dup, NC_000010.11:g.900930_900936dup, NC_000010.10:g.946868_946876del, NC_000010.10:g.946869_946876del, NC_000010.10:g.946871_946876del, NC_000010.10:g.946872_946876del, NC_000010.10:g.946873_946876del, NC_000010.10:g.946874_946876del, NC_000010.10:g.946875_946876del, NC_000010.10:g.946876del, NC_000010.10:g.946876dup, NC_000010.10:g.946875_946876dup, NC_000010.10:g.946874_946876dup, NC_000010.10:g.946873_946876dup, NC_000010.10:g.946872_946876dup, NC_000010.10:g.946871_946876dup, NC_000010.10:g.946870_946876dup

Select item 149117450810.

rs1491174508 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->ATTT [Show Flanks]
Chromosome:: 10:900920 (GRCh38)
10:946861 (GRCh37)
Canonical SPDI:: NC_000010.11:900920:TTT:TTTATTT
Gene:: LARP4B (Varview)
Functional Consequence:: upstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TTTATTT=0./0 (ALFA)
TTTA=0.00003/2 (GnomAD)
HGVS:: NC_000010.11:g.900923_900924insATTT, NC_000010.10:g.946863_946864insATTT

Select item 149115612711.

rs1491156127 has merged into rs547831151 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAA>-,A,AA,AAA,AAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA [Show Flanks]
Chromosome:: 10:888346 (GRCh38)
10:934286 (GRCh37)
Canonical SPDI:: NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:888337:AAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA
Gene:: LARP4B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
-=0.00003/8 (TOPMED)
C=0.030751/154 (1000Genomes)
HGVS:: NC_000010.11:g.888346_888350del, NC_000010.11:g.888347_888350del, NC_000010.11:g.888348_888350del, NC_000010.11:g.888349_888350del, NC_000010.11:g.888350del, NC_000010.11:g.888350dup, NC_000010.11:g.888349_888350dup, NC_000010.11:g.888348_888350dup, NC_000010.11:g.888347_888350dup, NC_000010.11:g.888346_888350dup, NC_000010.11:g.888345_888350dup, NC_000010.10:g.934286_934290del, NC_000010.10:g.934287_934290del, NC_000010.10:g.934288_934290del, NC_000010.10:g.934289_934290del, NC_000010.10:g.934290del, NC_000010.10:g.934290dup, NC_000010.10:g.934289_934290dup, NC_000010.10:g.934288_934290dup, NC_000010.10:g.934287_934290dup, NC_000010.10:g.934286_934290dup, NC_000010.10:g.934285_934290dup

Select item 149114878712.

rs1491148787 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:883785 (GRCh38)
10:929725 (GRCh37)
Canonical SPDI:: NC_000010.11:883783:ACA:A
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
-=0.000029/4 (GnomAD)
HGVS:: NC_000010.11:g.883785_883786del, NC_000010.10:g.929725_929726del

Select item 149114618613.

rs1491146186 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:863226 (GRCh38)
10:909166 (GRCh37)
Canonical SPDI:: NC_000010.11:863225:AT:
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.000636/10 (ALFA)
-=0.001058/143 (GnomAD)
-=0.01946/75 (ALSPAC)
-=0.020496/76 (TWINSUK)
HGVS:: NC_000010.11:g.863226_863227del, NC_000010.10:g.909166_909167del

Select item 149111300614.

rs1491113006 has merged into rs141536087 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACACACACACACACAC>-,ACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC [Show Flanks]
Chromosome:: 10:808753 (GRCh38)
10:854693 (GRCh37)
Canonical SPDI:: NC_000010.11:808751:CACACACACACACACAC:C,NC_000010.11:808751:CACACACACACACACAC:CACACAC,NC_000010.11:808751:CACACACACACACACAC:CACACACACAC,NC_000010.11:808751:CACACACACACACACAC:CACACACACACAC,NC_000010.11:808751:CACACACACACACACAC:CACACACACACACAC,NC_000010.11:808751:CACACACACACACACAC:CACACACACACACACACAC,NC_000010.11:808751:CACACACACACACACAC:CACACACACACACACACACAC,NC_000010.11:808751:CACACACACACACACAC:CACACACACACACACACACACAC
Gene:: LARP4B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CACACAC=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.02932/113 (ALSPAC)
-=0.030475/113 (TWINSUK)
HGVS:: NC_000010.11:g.808753_808768del, NC_000010.11:g.808753AC[3], NC_000010.11:g.808753AC[5], NC_000010.11:g.808753AC[6], NC_000010.11:g.808753AC[7], NC_000010.11:g.808753AC[9], NC_000010.11:g.808753AC[10], NC_000010.11:g.808753AC[11], NC_000010.10:g.854693_854708del, NC_000010.10:g.854693AC[3], NC_000010.10:g.854693AC[5], NC_000010.10:g.854693AC[6], NC_000010.10:g.854693AC[7], NC_000010.10:g.854693AC[9], NC_000010.10:g.854693AC[10], NC_000010.10:g.854693AC[11], XM_017015990.2:c.*4159_*4174del, XM_017015990.2:c.*4159TG[3], XM_017015990.2:c.*4159TG[5], XM_017015990.2:c.*4159TG[6], XM_017015990.2:c.*4159TG[7], XM_017015990.2:c.*4159TG[9], XM_017015990.2:c.*4159TG[10], XM_017015990.2:c.*4159TG[11], XM_017015987.2:c.*4159_*4174del, XM_017015987.2:c.*4159TG[3], XM_017015987.2:c.*4159TG[5], XM_017015987.2:c.*4159TG[6], XM_017015987.2:c.*4159TG[7], XM_017015987.2:c.*4159TG[9], XM_017015987.2:c.*4159TG[10], XM_017015987.2:c.*4159TG[11], XM_017015988.2:c.*4159_*4174del, XM_017015988.2:c.*4159TG[3], XM_017015988.2:c.*4159TG[5], XM_017015988.2:c.*4159TG[6], XM_017015988.2:c.*4159TG[7], XM_017015988.2:c.*4159TG[9], XM_017015988.2:c.*4159TG[10], XM_017015988.2:c.*4159TG[11], NM_001351277.2:c.*4159_*4174del, NM_001351277.2:c.*4159TG[3], NM_001351277.2:c.*4159TG[5], NM_001351277.2:c.*4159TG[6], NM_001351277.2:c.*4159TG[7], NM_001351277.2:c.*4159TG[9], NM_001351277.2:c.*4159TG[10], NM_001351277.2:c.*4159TG[11], NM_001351277.1:c.*4159_*4174del, NM_001351277.1:c.*4159TG[3], NM_001351277.1:c.*4159TG[5], NM_001351277.1:c.*4159TG[6], NM_001351277.1:c.*4159TG[7], NM_001351277.1:c.*4159TG[9], NM_001351277.1:c.*4159TG[10], NM_001351277.1:c.*4159TG[11], NM_015155.2:c.*4159_*4174del, NM_015155.2:c.*4159TG[3], NM_015155.2:c.*4159TG[5], NM_015155.2:c.*4159TG[6], NM_015155.2:c.*4159TG[7], NM_015155.2:c.*4159TG[9], NM_015155.2:c.*4159TG[10], NM_015155.2:c.*4159TG[11], XM_017015992.2:c.*4159_*4174del, XM_017015992.2:c.*4159TG[3], XM_017015992.2:c.*4159TG[5], XM_017015992.2:c.*4159TG[6], XM_017015992.2:c.*4159TG[7], XM_017015992.2:c.*4159TG[9], XM_017015992.2:c.*4159TG[10], XM_017015992.2:c.*4159TG[11], XM_047424892.1:c.*4159_*4174del, XM_047424892.1:c.*4159TG[3], XM_047424892.1:c.*4159TG[5], XM_047424892.1:c.*4159TG[6], XM_047424892.1:c.*4159TG[7], XM_047424892.1:c.*4159TG[9], XM_047424892.1:c.*4159TG[10], XM_047424892.1:c.*4159TG[11], XM_047424896.1:c.*4159_*4174del, XM_047424896.1:c.*4159TG[3], XM_047424896.1:c.*4159TG[5], XM_047424896.1:c.*4159TG[6], XM_047424896.1:c.*4159TG[7], XM_047424896.1:c.*4159TG[9], XM_047424896.1:c.*4159TG[10], XM_047424896.1:c.*4159TG[11], XM_047424893.1:c.*4159_*4174del, XM_047424893.1:c.*4159TG[3], XM_047424893.1:c.*4159TG[5], XM_047424893.1:c.*4159TG[6], XM_047424893.1:c.*4159TG[7], XM_047424893.1:c.*4159TG[9], XM_047424893.1:c.*4159TG[10], XM_047424893.1:c.*4159TG[11], XM_047424895.1:c.*4159_*4174del, XM_047424895.1:c.*4159TG[3], XM_047424895.1:c.*4159TG[5], XM_047424895.1:c.*4159TG[6], XM_047424895.1:c.*4159TG[7], XM_047424895.1:c.*4159TG[9], XM_047424895.1:c.*4159TG[10], XM_047424895.1:c.*4159TG[11], XM_047424894.1:c.*4159_*4174del, XM_047424894.1:c.*4159TG[3], XM_047424894.1:c.*4159TG[5], XM_047424894.1:c.*4159TG[6], XM_047424894.1:c.*4159TG[7], XM_047424894.1:c.*4159TG[9], XM_047424894.1:c.*4159TG[10], XM_047424894.1:c.*4159TG[11], XM_047424897.1:c.*4159_*4174del, XM_047424897.1:c.*4159TG[3], XM_047424897.1:c.*4159TG[5], XM_047424897.1:c.*4159TG[6], XM_047424897.1:c.*4159TG[7], XM_047424897.1:c.*4159TG[9], XM_047424897.1:c.*4159TG[10], XM_047424897.1:c.*4159TG[11], XM_047424902.1:c.*4159_*4174del, XM_047424902.1:c.*4159TG[3], XM_047424902.1:c.*4159TG[5], XM_047424902.1:c.*4159TG[6], XM_047424902.1:c.*4159TG[7], XM_047424902.1:c.*4159TG[9], XM_047424902.1:c.*4159TG[10], XM_047424902.1:c.*4159TG[11]

Select item 149109639815.

rs1491096398 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 10:892902 (GRCh38)
10:938842 (GRCh37)
Canonical SPDI:: NC_000010.11:892901:AT:
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000010.11:g.892902_892903del, NC_000010.10:g.938842_938843del, XM_017015990.2:c.-2359_-2358del

Select item 149108371316.

rs1491083713 has merged into rs58452748 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:897998 (GRCh38)
10:943938 (GRCh37)
Canonical SPDI:: NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:897987:AAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LARP4B (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.096446/483 (1000Genomes)
HGVS:: NC_000010.11:g.897998_898014del, NC_000010.11:g.897999_898014del, NC_000010.11:g.898001_898014del, NC_000010.11:g.898002_898014del, NC_000010.11:g.898003_898014del, NC_000010.11:g.898004_898014del, NC_000010.11:g.898005_898014del, NC_000010.11:g.898006_898014del, NC_000010.11:g.898007_898014del, NC_000010.11:g.898008_898014del, NC_000010.11:g.898009_898014del, NC_000010.11:g.898010_898014del, NC_000010.11:g.898011_898014del, NC_000010.11:g.898012_898014del, NC_000010.11:g.898013_898014del, NC_000010.11:g.898014del, NC_000010.11:g.898014dup, NC_000010.11:g.898013_898014dup, NC_000010.11:g.898012_898014dup, NC_000010.11:g.898011_898014dup, NC_000010.11:g.898010_898014dup, NC_000010.11:g.898009_898014dup, NC_000010.11:g.898008_898014dup, NC_000010.11:g.898007_898014dup, NC_000010.11:g.898006_898014dup, NC_000010.11:g.898005_898014dup, NC_000010.11:g.898004_898014dup, NC_000010.11:g.898003_898014dup, NC_000010.11:g.898002_898014dup, NC_000010.11:g.898001_898014dup, NC_000010.11:g.897998_898014dup, NC_000010.11:g.897997_898014dup, NC_000010.11:g.897988_898014A[38]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000010.10:g.943938_943954del, NC_000010.10:g.943939_943954del, NC_000010.10:g.943941_943954del, NC_000010.10:g.943942_943954del, NC_000010.10:g.943943_943954del, NC_000010.10:g.943944_943954del, NC_000010.10:g.943945_943954del, NC_000010.10:g.943946_943954del, NC_000010.10:g.943947_943954del, NC_000010.10:g.943948_943954del, NC_000010.10:g.943949_943954del, NC_000010.10:g.943950_943954del, NC_000010.10:g.943951_943954del, NC_000010.10:g.943952_943954del, NC_000010.10:g.943953_943954del, NC_000010.10:g.943954del, NC_000010.10:g.943954dup, NC_000010.10:g.943953_943954dup, NC_000010.10:g.943952_943954dup, NC_000010.10:g.943951_943954dup, NC_000010.10:g.943950_943954dup, NC_000010.10:g.943949_943954dup, NC_000010.10:g.943948_943954dup, NC_000010.10:g.943947_943954dup, NC_000010.10:g.943946_943954dup, NC_000010.10:g.943945_943954dup, NC_000010.10:g.943944_943954dup, NC_000010.10:g.943943_943954dup, NC_000010.10:g.943942_943954dup, NC_000010.10:g.943941_943954dup, NC_000010.10:g.943938_943954dup, NC_000010.10:g.943937_943954dup, NC_000010.10:g.943928_943954A[38]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], XM_017015990.2:c.-7460_-7444del, XM_017015990.2:c.-7459_-7444del, XM_017015990.2:c.-7457_-7444del, XM_017015990.2:c.-7456_-7444del, XM_017015990.2:c.-7455_-7444del, XM_017015990.2:c.-7454_-7444del, XM_017015990.2:c.-7453_-7444del, XM_017015990.2:c.-7452_-7444del, XM_017015990.2:c.-7451_-7444del, XM_017015990.2:c.-7450_-7444del, XM_017015990.2:c.-7449_-7444del, XM_017015990.2:c.-7448_-7444del, XM_017015990.2:c.-7447_-7444del, XM_017015990.2:c.-7446_-7444del, XM_017015990.2:c.-7445_-7444del, XM_017015990.2:c.-7444del, XM_017015990.2:c.-7444dup, XM_017015990.2:c.-7445_-7444dup, XM_017015990.2:c.-7446_-7444dup, XM_017015990.2:c.-7447_-7444dup, XM_017015990.2:c.-7448_-7444dup, XM_017015990.2:c.-7449_-7444dup, XM_017015990.2:c.-7450_-7444dup, XM_017015990.2:c.-7451_-7444dup, XM_017015990.2:c.-7452_-7444dup, XM_017015990.2:c.-7453_-7444dup, XM_017015990.2:c.-7454_-7444dup, XM_017015990.2:c.-7455_-7444dup, XM_017015990.2:c.-7456_-7444dup, XM_017015990.2:c.-7457_-7444dup, XM_017015990.2:c.-7460_-7444dup, XM_017015990.2:c.-7461_-7444dup, XM_017015990.2:c.-7470_-7444T[37]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 149106995517.

rs1491069955 has merged into rs10661482 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAA>-,AA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAACCAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:862266 (GRCh38)
10:908206 (GRCh37)
Canonical SPDI:: NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:862256:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LARP4B (Varview)
Functional Consequence:: genic_downstream_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.862266_862281del, NC_000010.11:g.862268_862281del, NC_000010.11:g.862270_862281del, NC_000010.11:g.862271_862281del, NC_000010.11:g.862272_862281del, NC_000010.11:g.862273_862281del, NC_000010.11:g.862274_862281del, NC_000010.11:g.862275_862281del, NC_000010.11:g.862276_862281del, NC_000010.11:g.862277_862281del, NC_000010.11:g.862278_862281del, NC_000010.11:g.862279_862281del, NC_000010.11:g.862280_862281del, NC_000010.11:g.862281del, NC_000010.11:g.862281dup, NC_000010.11:g.862280_862281dup, NC_000010.11:g.862279_862281dup, NC_000010.11:g.862278_862281dup, NC_000010.11:g.862277_862281dup, NC_000010.11:g.862276_862281dup, NC_000010.11:g.862275_862281dup, NC_000010.11:g.862274_862281dup, NC_000010.11:g.862273_862281dup, NC_000010.11:g.862272_862281dup, NC_000010.11:g.862271_862281dup, NC_000010.11:g.862270_862281dup, NC_000010.11:g.862269_862281dup, NC_000010.11:g.862268_862281dup, NC_000010.11:g.862267_862281dup, NC_000010.11:g.862266_862281dup, NC_000010.11:g.862264_862281dup, NC_000010.11:g.862263_862281dup, NC_000010.11:g.862262_862281dup, NC_000010.11:g.862261_862281dup, NC_000010.11:g.862260_862281dup, NC_000010.11:g.862259_862281dup, NC_000010.11:g.862258_862281dup, NC_000010.11:g.862257_862281dup, NC_000010.11:g.862281_862282insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.862281_862282insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.862281_862282insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.862281_862282insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.11:g.862257_862281A[31]CCAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000010.10:g.908206_908221del, NC_000010.10:g.908208_908221del, NC_000010.10:g.908210_908221del, NC_000010.10:g.908211_908221del, NC_000010.10:g.908212_908221del, NC_000010.10:g.908213_908221del, NC_000010.10:g.908214_908221del, NC_000010.10:g.908215_908221del, NC_000010.10:g.908216_908221del, NC_000010.10:g.908217_908221del, NC_000010.10:g.908218_908221del, NC_000010.10:g.908219_908221del, NC_000010.10:g.908220_908221del, NC_000010.10:g.908221del, NC_000010.10:g.908221dup, NC_000010.10:g.908220_908221dup, NC_000010.10:g.908219_908221dup, NC_000010.10:g.908218_908221dup, NC_000010.10:g.908217_908221dup, NC_000010.10:g.908216_908221dup, NC_000010.10:g.908215_908221dup, NC_000010.10:g.908214_908221dup, NC_000010.10:g.908213_908221dup, NC_000010.10:g.908212_908221dup, NC_000010.10:g.908211_908221dup, NC_000010.10:g.908210_908221dup, NC_000010.10:g.908209_908221dup, NC_000010.10:g.908208_908221dup, NC_000010.10:g.908207_908221dup, NC_000010.10:g.908206_908221dup, NC_000010.10:g.908204_908221dup, NC_000010.10:g.908203_908221dup, NC_000010.10:g.908202_908221dup, NC_000010.10:g.908201_908221dup, NC_000010.10:g.908200_908221dup, NC_000010.10:g.908199_908221dup, NC_000010.10:g.908198_908221dup, NC_000010.10:g.908197_908221dup, NC_000010.10:g.908221_908222insAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.908221_908222insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.908221_908222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.908221_908222insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000010.10:g.908197_908221A[31]CCAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]

Select item 149100582318.

rs1491005823 has merged into rs56787174 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:909302 (GRCh38)
10:955242 (GRCh37)
Canonical SPDI:: NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:909293:AAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LARP4B (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.225439/1129 (1000Genomes)
HGVS:: NC_000010.11:g.909302_909312del, NC_000010.11:g.909303_909312del, NC_000010.11:g.909304_909312del, NC_000010.11:g.909305_909312del, NC_000010.11:g.909306_909312del, NC_000010.11:g.909307_909312del, NC_000010.11:g.909308_909312del, NC_000010.11:g.909309_909312del, NC_000010.11:g.909310_909312del, NC_000010.11:g.909311_909312del, NC_000010.11:g.909312del, NC_000010.11:g.909312dup, NC_000010.11:g.909311_909312dup, NC_000010.11:g.909310_909312dup, NC_000010.11:g.909309_909312dup, NC_000010.11:g.909307_909312dup, NC_000010.11:g.909295_909312dup, NC_000010.10:g.955242_955252del, NC_000010.10:g.955243_955252del, NC_000010.10:g.955244_955252del, NC_000010.10:g.955245_955252del, NC_000010.10:g.955246_955252del, NC_000010.10:g.955247_955252del, NC_000010.10:g.955248_955252del, NC_000010.10:g.955249_955252del, NC_000010.10:g.955250_955252del, NC_000010.10:g.955251_955252del, NC_000010.10:g.955252del, NC_000010.10:g.955252dup, NC_000010.10:g.955251_955252dup, NC_000010.10:g.955250_955252dup, NC_000010.10:g.955249_955252dup, NC_000010.10:g.955247_955252dup, NC_000010.10:g.955235_955252dup

Select item 149100209419.

rs1491002094 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 10:930466 (GRCh38)
10:976406 (GRCh37)
Canonical SPDI:: NC_000010.11:930465:C:
Gene:: LARP4B (Varview), LOC124902363 (Varview)
Functional Consequence:: upstream_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.930466del, NC_000010.10:g.976406del

Select item 149099305320.

rs1490993053 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:855155 (GRCh38)
10:901095 (GRCh37)
Canonical SPDI:: NC_000010.11:855154:C:A
Gene:: LARP4B (Varview)
Functional Consequence:: genic_upstream_transcript_variant,genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.855155C>A, NC_000010.10:g.901095C>A

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