SNP Links for Gene (Select 10972) - SNP

Links from Gene

Items: 1 to 20 of 1000

<< First< Prev

Page of 50

Next >Last >>

Select item 14915659691.

rs1491565969 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 14:75132396 (GRCh38)
14:75599099 (GRCh37)
Canonical SPDI:: NC_000014.9:75132395:CA:
Gene:: TMED10 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.018995/307 (ALFA)
-=0.000886/15 (TOMMO)
-=0.021049/2301 (GnomAD)
-=0.047297/28 (NorthernSweden)
-=0.0952/353 (TWINSUK)
-=0.098599/380 (ALSPAC)
-=0.25/10 (GENOME_DK)
HGVS:: NC_000014.9:g.75132396_75132397del, NC_000014.8:g.75599099_75599100del, NM_006827.6:c.*2488_*2489del, NM_006827.5:c.*2488_*2489del

Select item 14915378662.

rs1491537866 [Homo sapiens]

Variant type:: INS
Alleles:: ->A,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA,ATATATATATATATA,ATATATATATATATATA,ATATATATATATATATATATATA,G [Show Flanks]
Chromosome:: 14:75164578 (GRCh38)
14:75631282 (GRCh37)
Canonical SPDI:: NC_000014.9:75164578::A,NC_000014.9:75164578::ATA,NC_000014.9:75164578::ATATA,NC_000014.9:75164578::ATATATA,NC_000014.9:75164578::ATATATATA,NC_000014.9:75164578::ATATATATATA,NC_000014.9:75164578::ATATATATATATATA,NC_000014.9:75164578::ATATATATATATATATA,NC_000014.9:75164578::ATATATATATATATATATATATA,NC_000014.9:75164578::G
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATA=0./0 (ALFA)
HGVS:: NC_000014.9:g.75164578_75164579insA, NC_000014.9:g.75164578_75164579insATA, NC_000014.9:g.75164578_75164579insATATA, NC_000014.9:g.75164578_75164579insATATATA, NC_000014.9:g.75164578_75164579insATATATATA, NC_000014.9:g.75164578_75164579insATATATATATA, NC_000014.9:g.75164578_75164579insATATATATATATATA, NC_000014.9:g.75164578_75164579insATATATATATATATATA, NC_000014.9:g.75164578_75164579insATATATATATATATATATATATA, NC_000014.9:g.75164578_75164579insG, NC_000014.8:g.75631281_75631282insA, NC_000014.8:g.75631281_75631282insATA, NC_000014.8:g.75631281_75631282insATATA, NC_000014.8:g.75631281_75631282insATATATA, NC_000014.8:g.75631281_75631282insATATATATA, NC_000014.8:g.75631281_75631282insATATATATATA, NC_000014.8:g.75631281_75631282insATATATATATATATA, NC_000014.8:g.75631281_75631282insATATATATATATATATA, NC_000014.8:g.75631281_75631282insATATATATATATATATATATATA, NC_000014.8:g.75631281_75631282insG

Select item 14915364863.

rs1491536486 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 14:75166939 (GRCh38)
14:75633642 (GRCh37)
Canonical SPDI:: NC_000014.9:75166938:CT:
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000014.9:g.75166939_75166940del, NC_000014.8:g.75633642_75633643del

Select item 14915238474.

rs1491523847 [Homo sapiens]

Variant type:: DEL
Alleles:: TC>- [Show Flanks]
Chromosome:: 14:75132384 (GRCh38)
14:75599087 (GRCh37)
Canonical SPDI:: NC_000014.9:75132383:TC:
Gene:: TMED10 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: -=0.00008/1 (ALFA)
HGVS:: NC_000014.9:g.75132384_75132385del, NC_000014.8:g.75599087_75599088del, NM_006827.6:c.*2500_*2501del, NM_006827.5:c.*2500_*2501del

Select item 14914938425.

rs1491493842 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CT [Show Flanks]
Chromosome:: 14:75138813 (GRCh38)
14:75605517 (GRCh37)
Canonical SPDI:: NC_000014.9:75138813:T:TCT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TCT=0./0 (ALFA)
TC=0.00149/4 (GnomAD)
HGVS:: NC_000014.9:g.75138814_75138815insCT, NC_000014.8:g.75605517_75605518insCT

Select item 14914828296.

rs1491482829 has merged into rs368437388 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT,TTTTTT,TTTTTTT [Show Flanks]
Chromosome:: 14:75137722 (GRCh38)
14:75604425 (GRCh37)
Canonical SPDI:: NC_000014.9:75137708:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:75137708:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:75137708:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:75137708:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:75137708:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:75137708:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:75137708:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
T=0.19108/3193 (TOMMO)
T=0.48083/2408 (1000Genomes)
HGVS:: NC_000014.9:g.75137722_75137724del, NC_000014.9:g.75137723_75137724del, NC_000014.9:g.75137724del, NC_000014.9:g.75137724dup, NC_000014.9:g.75137723_75137724dup, NC_000014.9:g.75137722_75137724dup, NC_000014.9:g.75137721_75137724dup, NC_000014.8:g.75604425_75604427del, NC_000014.8:g.75604426_75604427del, NC_000014.8:g.75604427del, NC_000014.8:g.75604427dup, NC_000014.8:g.75604426_75604427dup, NC_000014.8:g.75604425_75604427dup, NC_000014.8:g.75604424_75604427dup

Select item 14914658737.

rs1491465873 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 14:75137691 (GRCh38)
14:75604395 (GRCh37)
Canonical SPDI:: NC_000014.9:75137691:TT:TTT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTT=0.01973/235 (ALFA)
T=0.022898/383 (TOMMO)
T=0.025733/3226 (GnomAD)
T=0.095186/174 (Korea1K)
HGVS:: NC_000014.9:g.75137693dup, NC_000014.8:g.75604396dup

Select item 14913532318.

rs1491353231 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTTTTTTTTTTTT,GTTTTTTTTTTTTT,GTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:75147185 (GRCh38)
14:75613889 (GRCh37)
Canonical SPDI:: NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75147185:TTTTTTTTTT:TTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTGTTTTTTTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.9:g.75147186_75147195T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000014.8:g.75613889_75613898T[10]GTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14913492489.

rs1491349248 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 14:75178155 (GRCh38)
14:75644859 (GRCh37)
Canonical SPDI:: NC_000014.9:75178155::G
Gene:: TMED10 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000033/1 (GnomAD)
HGVS:: NC_000014.9:g.75178155_75178156insG, NC_000014.8:g.75644858_75644859insG

Select item 149131603410.

rs1491316034 has merged into rs11366602 [Homo sapiens]

Variant type:: DELINS
Alleles:: TT>-,T,TTT,TTTT [Show Flanks]
Chromosome:: 14:75178165 (GRCh38)
14:75644868 (GRCh37)
Canonical SPDI:: NC_000014.9:75178154:TTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:75178154:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:75178154:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:75178154:TTTTTTTTTTTT:TTTTTTTTTTTTTT
Gene:: TMED10 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTT=0./0 (ALFA)
T=0.325/13 (GENOME_DK)
-=0.4557/2282 (1000Genomes)
T=0.4625/1715 (TWINSUK)
T=0.4811/1854 (ALSPAC)
HGVS:: NC_000014.9:g.75178165_75178166del, NC_000014.9:g.75178166del, NC_000014.9:g.75178166dup, NC_000014.9:g.75178165_75178166dup, NC_000014.8:g.75644868_75644869del, NC_000014.8:g.75644869del, NC_000014.8:g.75644869dup, NC_000014.8:g.75644868_75644869dup

Select item 149129028411.

rs1491290284 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 14:75137691 (GRCh38)
14:75604394 (GRCh37)
Canonical SPDI:: NC_000014.9:75137690:AT:
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.00202/24 (ALFA)
HGVS:: NC_000014.9:g.75137691_75137692del, NC_000014.8:g.75604394_75604395del

Select item 149120982512.

rs1491209825 has merged into rs59707221 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:75138820 (GRCh38)
14:75605523 (GRCh37)
Canonical SPDI:: NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75138812:TTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.75138820_75138832del, NC_000014.9:g.75138823_75138832del, NC_000014.9:g.75138824_75138832del, NC_000014.9:g.75138825_75138832del, NC_000014.9:g.75138826_75138832del, NC_000014.9:g.75138827_75138832del, NC_000014.9:g.75138828_75138832del, NC_000014.9:g.75138829_75138832del, NC_000014.9:g.75138830_75138832del, NC_000014.9:g.75138831_75138832del, NC_000014.9:g.75138832del, NC_000014.9:g.75138832dup, NC_000014.9:g.75138831_75138832dup, NC_000014.9:g.75138830_75138832dup, NC_000014.9:g.75138829_75138832dup, NC_000014.9:g.75138828_75138832dup, NC_000014.9:g.75138827_75138832dup, NC_000014.9:g.75138826_75138832dup, NC_000014.9:g.75138825_75138832dup, NC_000014.9:g.75138824_75138832dup, NC_000014.9:g.75138823_75138832dup, NC_000014.9:g.75138822_75138832dup, NC_000014.9:g.75138821_75138832dup, NC_000014.9:g.75138820_75138832dup, NC_000014.9:g.75138819_75138832dup, NC_000014.9:g.75138818_75138832dup, NC_000014.9:g.75138817_75138832dup, NC_000014.9:g.75138816_75138832dup, NC_000014.9:g.75138815_75138832dup, NC_000014.9:g.75138814_75138832dup, NC_000014.9:g.75138813_75138832dup, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.9:g.75138832_75138833insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605523_75605535del, NC_000014.8:g.75605526_75605535del, NC_000014.8:g.75605527_75605535del, NC_000014.8:g.75605528_75605535del, NC_000014.8:g.75605529_75605535del, NC_000014.8:g.75605530_75605535del, NC_000014.8:g.75605531_75605535del, NC_000014.8:g.75605532_75605535del, NC_000014.8:g.75605533_75605535del, NC_000014.8:g.75605534_75605535del, NC_000014.8:g.75605535del, NC_000014.8:g.75605535dup, NC_000014.8:g.75605534_75605535dup, NC_000014.8:g.75605533_75605535dup, NC_000014.8:g.75605532_75605535dup, NC_000014.8:g.75605531_75605535dup, NC_000014.8:g.75605530_75605535dup, NC_000014.8:g.75605529_75605535dup, NC_000014.8:g.75605528_75605535dup, NC_000014.8:g.75605527_75605535dup, NC_000014.8:g.75605526_75605535dup, NC_000014.8:g.75605525_75605535dup, NC_000014.8:g.75605524_75605535dup, NC_000014.8:g.75605523_75605535dup, NC_000014.8:g.75605522_75605535dup, NC_000014.8:g.75605521_75605535dup, NC_000014.8:g.75605520_75605535dup, NC_000014.8:g.75605519_75605535dup, NC_000014.8:g.75605518_75605535dup, NC_000014.8:g.75605517_75605535dup, NC_000014.8:g.75605516_75605535dup, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000014.8:g.75605535_75605536insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 149109114113.

rs1491091141 has merged into rs60845992 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTTTTTTTT>-,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 14:75164584 (GRCh38)
14:75631287 (GRCh37)
Canonical SPDI:: NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000014.9:75164577:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTT=0./0 (ALFA)
HGVS:: NC_000014.9:g.75164584_75164594del, NC_000014.9:g.75164586_75164594del, NC_000014.9:g.75164587_75164594del, NC_000014.9:g.75164588_75164594del, NC_000014.9:g.75164589_75164594del, NC_000014.9:g.75164590_75164594del, NC_000014.9:g.75164591_75164594del, NC_000014.9:g.75164592_75164594del, NC_000014.9:g.75164593_75164594del, NC_000014.9:g.75164594del, NC_000014.9:g.75164594dup, NC_000014.9:g.75164593_75164594dup, NC_000014.9:g.75164592_75164594dup, NC_000014.9:g.75164591_75164594dup, NC_000014.9:g.75164590_75164594dup, NC_000014.9:g.75164589_75164594dup, NC_000014.9:g.75164588_75164594dup, NC_000014.9:g.75164587_75164594dup, NC_000014.9:g.75164586_75164594dup, NC_000014.9:g.75164585_75164594dup, NC_000014.9:g.75164584_75164594dup, NC_000014.9:g.75164583_75164594dup, NC_000014.9:g.75164582_75164594dup, NC_000014.9:g.75164581_75164594dup, NC_000014.8:g.75631287_75631297del, NC_000014.8:g.75631289_75631297del, NC_000014.8:g.75631290_75631297del, NC_000014.8:g.75631291_75631297del, NC_000014.8:g.75631292_75631297del, NC_000014.8:g.75631293_75631297del, NC_000014.8:g.75631294_75631297del, NC_000014.8:g.75631295_75631297del, NC_000014.8:g.75631296_75631297del, NC_000014.8:g.75631297del, NC_000014.8:g.75631297dup, NC_000014.8:g.75631296_75631297dup, NC_000014.8:g.75631295_75631297dup, NC_000014.8:g.75631294_75631297dup, NC_000014.8:g.75631293_75631297dup, NC_000014.8:g.75631292_75631297dup, NC_000014.8:g.75631291_75631297dup, NC_000014.8:g.75631290_75631297dup, NC_000014.8:g.75631289_75631297dup, NC_000014.8:g.75631288_75631297dup, NC_000014.8:g.75631287_75631297dup, NC_000014.8:g.75631286_75631297dup, NC_000014.8:g.75631285_75631297dup, NC_000014.8:g.75631284_75631297dup

Select item 149101978214.

rs1491019782 has merged into rs377453522 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTT>-,T,TT,TTTT,TTTTT [Show Flanks]
Chromosome:: 14:75171295 (GRCh38)
14:75637998 (GRCh37)
Canonical SPDI:: NC_000014.9:75171281:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000014.9:75171281:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000014.9:75171281:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000014.9:75171281:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000014.9:75171281:TTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTTTT=0./0 (ALFA)
T=0.03333/20 (NorthernSweden)
HGVS:: NC_000014.9:g.75171295_75171297del, NC_000014.9:g.75171296_75171297del, NC_000014.9:g.75171297del, NC_000014.9:g.75171297dup, NC_000014.9:g.75171296_75171297dup, NC_000014.8:g.75637998_75638000del, NC_000014.8:g.75637999_75638000del, NC_000014.8:g.75638000del, NC_000014.8:g.75638000dup, NC_000014.8:g.75637999_75638000dup

Select item 149091499015.

rs1490914990 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:75134562 (GRCh38)
14:75601265 (GRCh37)
Canonical SPDI:: NC_000014.9:75134561:A:G
Gene:: TMED10 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.75134562A>G, NC_000014.8:g.75601265A>G, NM_006827.6:c.*323T>C, NM_006827.5:c.*323T>C

Select item 149067916516.

rs1490679165 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:75165402 (GRCh38)
14:75632105 (GRCh37)
Canonical SPDI:: NC_000014.9:75165401:A:G
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.75165402A>G, NC_000014.8:g.75632105A>G

Select item 149065466817.

rs1490654668 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>C
Chromosome:: no mapping
Canonical SPDI:

Select item 149064396118.

rs1490643961 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 14:75140381 (GRCh38)
14:75607084 (GRCh37)
Canonical SPDI:: NC_000014.9:75140380:G:A,NC_000014.9:75140380:G:T
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.75140381G>A, NC_000014.9:g.75140381G>T, NC_000014.8:g.75607084G>A, NC_000014.8:g.75607084G>T

Select item 149062910219.

rs1490629102 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->CATA [Show Flanks]
Chromosome:: 14:75146926 (GRCh38)
14:75613630 (GRCh37)
Canonical SPDI:: NC_000014.9:75146926:ATA:ATACATA
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ATACATA=0./0 (ALFA)
ATAC=0.000136/19 (GnomAD)
ATAC=0.007096/13 (Korea1K)
ATAC=0.011077/186 (TOMMO)
HGVS:: NC_000014.9:g.75146929_75146930insCATA, NC_000014.8:g.75613632_75613633insCATA

Select item 149051506420.

rs1490515064 has merged into rs200928514 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>-,TT [Show Flanks]
Chromosome:: 14:75165240 (GRCh38)
14:75631943 (GRCh37)
Canonical SPDI:: NC_000014.9:75165239:TTTTTTTTT:TTTTTTTT,NC_000014.9:75165239:TTTTTTTTT:TTTTTTTTTT
Gene:: TMED10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTT=0./0 (ALFA)
-=0.00032/5 (TOMMO)
HGVS:: NC_000014.9:g.75165248del, NC_000014.9:g.75165248dup, NC_000014.8:g.75631951del, NC_000014.8:g.75631951dup

<< First< Prev

Page of 50

Next >Last >>

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 1000

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity