SNP Links for Gene (Select 7366) - SNP

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Select item 14915869311.

rs1491586931 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 4:68650994 (GRCh38)
4:69516713 (GRCh37)
Canonical SPDI:: NC_000004.12:68650994:G:GG
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
G=0.00003/2 (GnomAD)
HGVS:: NC_000004.12:g.68650995dup, NC_000004.11:g.69516713dup, NG_052676.1:g.24782dup, NT_167250.2:g.227352dup, NT_167250.1:g.229302dup

Select item 14913754762.

rs1491375476 has merged into rs376333738 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTGCCTTTTTTTTGATTGTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:68651008 (GRCh38)
4:69516726 (GRCh37)
Canonical SPDI:: NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTCTTTTGCCTTTTTTTTGATTGTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000004.12:68650995:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
T=0.2971/1488 (1000Genomes)
HGVS:: NC_000004.12:g.68651008_68651012del, NC_000004.12:g.68651009_68651012del, NC_000004.12:g.68651010_68651012del, NC_000004.12:g.68651011_68651012del, NC_000004.12:g.68651012del, NC_000004.12:g.68651012dup, NC_000004.12:g.68651011_68651012dup, NC_000004.12:g.68651010_68651012dup, NC_000004.12:g.68651009_68651012dup, NC_000004.12:g.68651008_68651012dup, NC_000004.12:g.68650996_68651012T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.12:g.68651006_68651012dup, NC_000004.12:g.68651004_68651012dup, NC_000004.12:g.68651003_68651012dup, NC_000004.12:g.68650996_68651012T[45]CTTTTGCCTTTTTTTTGATTGTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.12:g.68651012_68651013insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.68651012_68651013insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.68651012_68651013insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.12:g.68651012_68651013insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.69516726_69516730del, NC_000004.11:g.69516727_69516730del, NC_000004.11:g.69516728_69516730del, NC_000004.11:g.69516729_69516730del, NC_000004.11:g.69516730del, NC_000004.11:g.69516730dup, NC_000004.11:g.69516729_69516730dup, NC_000004.11:g.69516728_69516730dup, NC_000004.11:g.69516727_69516730dup, NC_000004.11:g.69516726_69516730dup, NC_000004.11:g.69516714_69516730T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.11:g.69516724_69516730dup, NC_000004.11:g.69516722_69516730dup, NC_000004.11:g.69516721_69516730dup, NC_000004.11:g.69516714_69516730T[45]CTTTTGCCTTTTTTTTGATTGTTTTTTTTTTTTTTTTTTTTT[1], NC_000004.11:g.69516730_69516731insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.69516730_69516731insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.69516730_69516731insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000004.11:g.69516730_69516731insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_052676.1:g.24777_24781del, NG_052676.1:g.24778_24781del, NG_052676.1:g.24779_24781del, NG_052676.1:g.24780_24781del, NG_052676.1:g.24781del, NG_052676.1:g.24781dup, NG_052676.1:g.24780_24781dup, NG_052676.1:g.24779_24781dup, NG_052676.1:g.24778_24781dup, NG_052676.1:g.24777_24781dup, NG_052676.1:g.24765_24781A[26]TAAAAAAAAAAAAAAAAAAAAAA[1], NG_052676.1:g.24775_24781dup, NG_052676.1:g.24773_24781dup, NG_052676.1:g.24772_24781dup, NG_052676.1:g.24765_24781A[21]CAATCAAAAAAAAGGCAAAAGAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NG_052676.1:g.24781_24782insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052676.1:g.24781_24782insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052676.1:g.24781_24782insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NG_052676.1:g.24781_24782insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167250.2:g.227368dup, NT_167250.2:g.227365_227368del, NT_167250.2:g.227366_227368del, NT_167250.2:g.227367_227368del, NT_167250.2:g.227368del, NT_167250.2:g.227367_227368dup, NT_167250.2:g.227366_227368dup, NT_167250.2:g.227365_227368dup, NT_167250.2:g.227364_227368dup, NT_167250.2:g.227363_227368dup, NT_167250.2:g.227353_227368T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_167250.2:g.227361_227368dup, NT_167250.2:g.227359_227368dup, NT_167250.2:g.227358_227368dup, NT_167250.2:g.227353_227368T[45]CTTTTGCCTTTTTTTTGATTGTTTTTTTTTTTTTTTTTTTTT[1], NT_167250.2:g.227368_227369insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167250.2:g.227368_227369insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167250.2:g.227368_227369insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167250.2:g.227368_227369insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167250.1:g.229318dup, NT_167250.1:g.229315_229318del, NT_167250.1:g.229316_229318del, NT_167250.1:g.229317_229318del, NT_167250.1:g.229318del, NT_167250.1:g.229317_229318dup, NT_167250.1:g.229316_229318dup, NT_167250.1:g.229315_229318dup, NT_167250.1:g.229314_229318dup, NT_167250.1:g.229313_229318dup, NT_167250.1:g.229303_229318T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_167250.1:g.229311_229318dup, NT_167250.1:g.229309_229318dup, NT_167250.1:g.229308_229318dup, NT_167250.1:g.229303_229318T[45]CTTTTGCCTTTTTTTTGATTGTTTTTTTTTTTTTTTTTTTTT[1], NT_167250.1:g.229318_229319insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167250.1:g.229318_229319insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167250.1:g.229318_229319insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_167250.1:g.229318_229319insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Select item 14913752643.

rs1491375264 has merged into rs775748401 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT [Show Flanks]
Chromosome:: 4:68666761 (GRCh38)
4:69532479 (GRCh37)
Canonical SPDI:: NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000004.12:68666752:TTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTT=0./0 (ALFA)
HGVS:: NC_000004.12:g.68666761_68666764del, NC_000004.12:g.68666762_68666764del, NC_000004.12:g.68666763_68666764del, NC_000004.12:g.68666764del, NC_000004.12:g.68666764dup, NC_000004.12:g.68666763_68666764dup, NC_000004.12:g.68666762_68666764dup, NC_000004.12:g.68666761_68666764dup, NC_000004.12:g.68666760_68666764dup, NC_000004.12:g.68666759_68666764dup, NC_000004.12:g.68666758_68666764dup, NC_000004.12:g.68666757_68666764dup, NC_000004.12:g.68666756_68666764dup, NC_000004.11:g.69532479_69532482del, NC_000004.11:g.69532480_69532482del, NC_000004.11:g.69532481_69532482del, NC_000004.11:g.69532482del, NC_000004.11:g.69532482dup, NC_000004.11:g.69532481_69532482dup, NC_000004.11:g.69532480_69532482dup, NC_000004.11:g.69532479_69532482dup, NC_000004.11:g.69532478_69532482dup, NC_000004.11:g.69532477_69532482dup, NC_000004.11:g.69532476_69532482dup, NC_000004.11:g.69532475_69532482dup, NC_000004.11:g.69532474_69532482dup, NG_052676.1:g.9021_9024del, NG_052676.1:g.9022_9024del, NG_052676.1:g.9023_9024del, NG_052676.1:g.9024del, NG_052676.1:g.9024dup, NG_052676.1:g.9023_9024dup, NG_052676.1:g.9022_9024dup, NG_052676.1:g.9021_9024dup, NG_052676.1:g.9020_9024dup, NG_052676.1:g.9019_9024dup, NG_052676.1:g.9018_9024dup, NG_052676.1:g.9017_9024dup, NG_052676.1:g.9016_9024dup, NT_167250.2:g.243117_243120del, NT_167250.2:g.243118_243120del, NT_167250.2:g.243119_243120del, NT_167250.2:g.243120del, NT_167250.2:g.243120dup, NT_167250.2:g.243119_243120dup, NT_167250.2:g.243118_243120dup, NT_167250.2:g.243117_243120dup, NT_167250.2:g.243116_243120dup, NT_167250.2:g.243115_243120dup, NT_167250.2:g.243114_243120dup, NT_167250.2:g.243113_243120dup, NT_167250.2:g.243112_243120dup, NT_167250.1:g.245067_245070del, NT_167250.1:g.245068_245070del, NT_167250.1:g.245069_245070del, NT_167250.1:g.245070del, NT_167250.1:g.245070dup, NT_167250.1:g.245069_245070dup, NT_167250.1:g.245068_245070dup, NT_167250.1:g.245067_245070dup, NT_167250.1:g.245066_245070dup, NT_167250.1:g.245065_245070dup, NT_167250.1:g.245064_245070dup, NT_167250.1:g.245063_245070dup, NT_167250.1:g.245062_245070dup

Select item 14913701404.

rs1491370140 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGTT [Show Flanks]
Chromosome:: 4:68658928 (GRCh38)
4:69524647 (GRCh37)
Canonical SPDI:: NC_000004.12:68658928:AGTTAGTT:AGTTAGTTAGTT
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: AGTTAGTTAGTT=0./0 (ALFA)
AGTT=0.000011/3 (TOPMED)
HGVS:: NC_000004.12:g.68658929AGTT[3], NC_000004.11:g.69524647AGTT[3], NG_052676.1:g.16841AACT[3], NT_167250.2:g.235284AGTT[3], NT_167250.1:g.237234AGTT[3]

Select item 14911332445.

rs1491133244 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 4:68650995 (GRCh38)
4:69516713 (GRCh37)
Canonical SPDI:: NC_000004.12:68650993:TGT:T
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00025/3 (ALFA)
-=0.00004/1 (TOMMO)
-=0.00083/47 (GnomAD)
HGVS:: NC_000004.12:g.68650995_68650996del, NC_000004.11:g.69516713_69516714del, NG_052676.1:g.24782_24783del, NT_167250.2:g.227368dup, NT_167250.2:g.227352del, NT_167250.1:g.229318dup, NT_167250.1:g.229302del

Select item 14910401286.

rs1491040128 has merged into rs147929412 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT [Show Flanks]
Chromosome:: 4:68656403 (GRCh38)
4:69522121 (GRCh37)
Canonical SPDI:: NC_000004.12:68656391:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000004.12:68656391:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000004.12:68656391:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000004.12:68656391:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000004.12:68656391:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTT=0./0 (ALFA)
T=0.0049/19 (ALSPAC)
T=0.0067/25 (TWINSUK)
T=0.1544/92 (NorthernSweden)
T=0.25/10 (GENOME_DK)
HGVS:: NC_000004.12:g.68656403_68656406del, NC_000004.12:g.68656404_68656406del, NC_000004.12:g.68656405_68656406del, NC_000004.12:g.68656406del, NC_000004.12:g.68656406dup, NC_000004.11:g.69522121_69522124del, NC_000004.11:g.69522122_69522124del, NC_000004.11:g.69522123_69522124del, NC_000004.11:g.69522124del, NC_000004.11:g.69522124dup, NG_052676.1:g.19382_19385del, NG_052676.1:g.19383_19385del, NG_052676.1:g.19384_19385del, NG_052676.1:g.19385del, NG_052676.1:g.19385dup, NT_167250.2:g.232761dup, NT_167250.2:g.232759_232761del, NT_167250.2:g.232760_232761del, NT_167250.2:g.232761del, NT_167250.2:g.232760_232761dup, NT_167250.1:g.234711dup, NT_167250.1:g.234709_234711del, NT_167250.1:g.234710_234711del, NT_167250.1:g.234711del, NT_167250.1:g.234710_234711dup

Select item 14908418087.

rs1490841808 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:68646836 (GRCh38)
4:69512554 (GRCh37)
Canonical SPDI:: NC_000004.12:68646835:T:C
Gene:: UGT2B15 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000004.12:g.68646836T>C, NC_000004.11:g.69512554T>C, NG_052676.1:g.28941A>G, NM_001076.4:c.*268A>G, NM_001076.3:c.*268A>G, NT_167250.2:g.223204T>C, NT_167250.1:g.225154T>C

Select item 14904042838.

rs1490404283 [Homo sapiens]

Variant type:: DEL
Alleles:: ATA>- [Show Flanks]
Chromosome:: 4:68666748 (GRCh38)
4:69532466 (GRCh37)
Canonical SPDI:: NC_000004.12:68666747:ATA:
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00034/4 (ALFA)
-=0.00022/17 (GnomAD)
HGVS:: NC_000004.12:g.68666748_68666750del, NC_000004.11:g.69532466_69532468del, NG_052676.1:g.9027_9029del, NT_167250.2:g.243104_243106del, NT_167250.1:g.245054_245056del

Select item 14903811739.

rs1490381173 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:68653761 (GRCh38)
4:69519479 (GRCh37)
Canonical SPDI:: NC_000004.12:68653760:G:T
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.68653761G>T, NC_000004.11:g.69519479G>T, NG_052676.1:g.22016C>A, NT_167250.2:g.230117G>T, NT_167250.1:g.232067G>T

Select item 149031076310.

rs1490310763 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:68654105 (GRCh38)
4:69519823 (GRCh37)
Canonical SPDI:: NC_000004.12:68654104:A:G
Gene:: UGT2B15 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000026/7 (TOPMED)
G=0.000043/6 (GnomAD)
HGVS:: NC_000004.12:g.68654105A>G, NC_000004.11:g.69519823A>G, NG_052676.1:g.21672T>C, NM_001076.4:c.1245T>C, NM_001076.3:c.1245T>C, NT_167250.2:g.230461A>G, NT_167250.1:g.232411A>G

Select item 149025823711.

rs1490258237 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:68660817 (GRCh38)
4:69526535 (GRCh37)
Canonical SPDI:: NC_000004.12:68660816:G:A
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000036/5 (GnomAD)
HGVS:: NC_000004.12:g.68660817G>A, NC_000004.11:g.69526535G>A, NG_052676.1:g.14960C>T, NT_167250.2:g.237172G>A, NT_167250.1:g.239122G>A

Select item 149024003112.

rs1490240031 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:68666380 (GRCh38)
4:69532098 (GRCh37)
Canonical SPDI:: NC_000004.12:68666379:A:G
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.68666380A>G, NC_000004.11:g.69532098A>G, NG_052676.1:g.9397T>C, NT_167250.2:g.242736A>G, NT_167250.1:g.244686A>G

Select item 149022669813.

rs1490226698 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:68653360 (GRCh38)
4:69519078 (GRCh37)
Canonical SPDI:: NC_000004.12:68653359:T:C
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
C=0.000531/9 (TOMMO)
HGVS:: NC_000004.12:g.68653360T>C, NC_000004.11:g.69519078T>C, NG_052676.1:g.22417A>G, NT_167250.2:g.229716T>C, NT_167250.1:g.231666T>C

Select item 149018838914.

rs1490188389 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 4:68665497 (GRCh38)
4:69531215 (GRCh37)
Canonical SPDI:: NC_000004.12:68665496:C:G,NC_000004.12:68665496:C:T
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.68665497C>G, NC_000004.12:g.68665497C>T, NC_000004.11:g.69531215C>G, NC_000004.11:g.69531215C>T, NG_052676.1:g.10280G>C, NG_052676.1:g.10280G>A, NT_167250.2:g.241853C>G, NT_167250.2:g.241853C>T, NT_167250.1:g.243803C>G, NT_167250.1:g.243803C>T

Select item 149018226315.

rs1490182263 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:68660613 (GRCh38)
4:69526331 (GRCh37)
Canonical SPDI:: NC_000004.12:68660612:T:C
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.68660613T>C, NC_000004.11:g.69526331T>C, NG_052676.1:g.15164A>G, NT_167250.2:g.236968T>C, NT_167250.1:g.238918T>C

Select item 149010363916.

rs1490103639 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:68646995 (GRCh38)
4:69512713 (GRCh37)
Canonical SPDI:: NC_000004.12:68646994:A:G
Gene:: UGT2B15 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.68646995A>G, NC_000004.11:g.69512713A>G, NG_052676.1:g.28782T>C, NM_001076.4:c.*109T>C, NM_001076.3:c.*109T>C, NT_167250.2:g.223364A>G, NT_167250.1:g.225314A>G

Select item 149002141117.

rs1490021411 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:68672732 (GRCh38)
4:69538450 (GRCh37)
Canonical SPDI:: NC_000004.12:68672731:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.68672732C>T, NC_000004.11:g.69538450C>T, NG_052676.1:g.3045G>A, NT_167250.2:g.249087C>T, NT_167250.1:g.251037C>T

Select item 148999623318.

rs1489996233 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:68671950 (GRCh38)
4:69537668 (GRCh37)
Canonical SPDI:: NC_000004.12:68671949:A:G
Gene:: UGT2B15 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.68671950A>G, NC_000004.11:g.69537668A>G, NG_052676.1:g.3827T>C, NT_167250.2:g.248305A>G, NT_167250.1:g.250255A>G

Select item 148973742319.

rs1489737423 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 4:68650823 (GRCh38)
4:69516541 (GRCh37)
Canonical SPDI:: NC_000004.12:68650822:T:C,NC_000004.12:68650822:T:G
Gene:: UGT2B15 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.68650823T>C, NC_000004.12:g.68650823T>G, NC_000004.11:g.69516541T>C, NC_000004.11:g.69516541T>G, NG_052676.1:g.24954A>G, NG_052676.1:g.24954A>C, NT_167250.2:g.227180T>C, NT_167250.2:g.227180T>G, NT_167250.1:g.229130T>C, NT_167250.1:g.229130T>G

Select item 148960125820.

rs1489601258 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 4:68646238 (GRCh38)
4:69511956 (GRCh37)
Canonical SPDI:: NC_000004.12:68646237:C:G,NC_000004.12:68646237:C:T
Gene:: UGT2B15 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.68646238C>G, NC_000004.12:g.68646238C>T, NC_000004.11:g.69511956C>G, NC_000004.11:g.69511956C>T, NG_052676.1:g.29539G>C, NG_052676.1:g.29539G>A, NT_167250.2:g.222605C>G, NT_167250.2:g.222605C>T, NT_167250.1:g.224555C>G, NT_167250.1:g.224555C>T

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