SNP Links for Nucleotide (Select 656214670) - SNP

Links from Nucleotide

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Select item 14906458061.

rs1490645806 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:190065434 (GRCh38)
4:190986589 (GRCh37)
Canonical SPDI:: NC_000004.12:190065433:A:C
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00008/1 (ALFA)
C=0.00004/1 (TOMMO)
HGVS:: NC_000004.12:g.190065434A>C, NC_000004.11:g.190986589A>C, NW_015495300.1:g.158036A>C, NT_167222.1:g.70419A>C, NW_015495301.1:g.158036A>C, NW_003571034.1:g.158364A>C, NR_121644.1:n.933A>C

Select item 14901543632.

rs1490154363 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:190065313 (GRCh38)
4:190986468 (GRCh37)
Canonical SPDI:: NC_000004.12:190065312:C:A,NC_000004.12:190065312:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000004.12:g.190065313C>A, NC_000004.12:g.190065313C>T, NC_000004.11:g.190986468C>A, NC_000004.11:g.190986468C>T, NW_015495300.1:g.157917C>A, NW_015495300.1:g.157917C>T, NT_167222.1:g.70300C>A, NT_167222.1:g.70300C>T, NW_015495301.1:g.157917C>A, NW_015495301.1:g.157917C>T, NW_003571034.1:g.158243C>A, NW_003571034.1:g.158243C>T, NR_121644.1:n.812C>A, NR_121644.1:n.812C>T

Select item 14901217503.

rs1490121750 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 4:190065649 (GRCh38)
4:190986804 (GRCh37)
Canonical SPDI:: NC_000004.12:190065648:G:A,NC_000004.12:190065648:G:C,NC_000004.12:190065648:G:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00009/1 (ALFA)
T=0.01344/142 (TOMMO)
C=0.0235/44 (KOREAN)
G=0.5/3 (Siberian)
HGVS:: NC_000004.12:g.190065649G>A, NC_000004.12:g.190065649G>C, NC_000004.12:g.190065649G>T, NC_000004.11:g.190986804G>A, NC_000004.11:g.190986804G>C, NC_000004.11:g.190986804G>T, NW_015495300.1:g.158251G>A, NW_015495300.1:g.158251G>C, NW_015495300.1:g.158251G>T, NT_167222.1:g.70634G>A, NT_167222.1:g.70634G>C, NT_167222.1:g.70634G>T, NW_015495301.1:g.158251G>A, NW_015495301.1:g.158251G>C, NW_015495301.1:g.158251G>T, NW_003571034.1:g.158579G>A, NW_003571034.1:g.158579G>C, NW_003571034.1:g.158579G>T, NR_121644.1:n.1148G>A, NR_121644.1:n.1148G>C, NR_121644.1:n.1148G>T

Select item 14894214414.

rs1489421441 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 4:190067123 (GRCh38)
4:190988278 (GRCh37)
Canonical SPDI:: NC_000004.12:190067122:G:A,NC_000004.12:190067122:G:C,NC_000004.12:190067122:G:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.0102/88 (TOMMO)
A=0.0972/284 (KOREAN)
HGVS:: NC_000004.12:g.190067123G>A, NC_000004.12:g.190067123G>C, NC_000004.12:g.190067123G>T, NC_000004.11:g.190988278G>A, NC_000004.11:g.190988278G>C, NC_000004.11:g.190988278G>T, NW_015495300.1:g.159724G>A, NW_015495300.1:g.159724G>C, NW_015495300.1:g.159724G>T, NT_167222.1:g.72107G>A, NT_167222.1:g.72107G>C, NT_167222.1:g.72107G>T, NW_015495301.1:g.159724G>A, NW_015495301.1:g.159724G>C, NW_015495301.1:g.159724G>T, NW_003571034.1:g.160053G>A, NW_003571034.1:g.160053G>C, NW_003571034.1:g.160053G>T, NR_121644.1:n.2622G>A, NR_121644.1:n.2622G>C, NR_121644.1:n.2622G>T

Select item 14891435355.

rs1489143535 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 4:190066336 (GRCh38)
4:190987491 (GRCh37)
Canonical SPDI:: NC_000004.12:190066335:C:A,NC_000004.12:190066335:C:G,NC_000004.12:190066335:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0./0 (SGDP_PRJ)
T=0.0023/4 (TOMMO)
T=0.2516/238 (KOREAN)
HGVS:: NC_000004.12:g.190066336C>A, NC_000004.12:g.190066336C>G, NC_000004.12:g.190066336C>T, NC_000004.11:g.190987491C>A, NC_000004.11:g.190987491C>G, NC_000004.11:g.190987491C>T, NW_015495300.1:g.158938C>A, NW_015495300.1:g.158938C>G, NW_015495300.1:g.158938C>T, NT_167222.1:g.71321C>A, NT_167222.1:g.71321C>G, NT_167222.1:g.71321C>T, NW_015495301.1:g.158938C>A, NW_015495301.1:g.158938C>G, NW_015495301.1:g.158938C>T, NW_003571034.1:g.159266C>A, NW_003571034.1:g.159266C>G, NW_003571034.1:g.159266C>T, NR_121644.1:n.1835C>A, NR_121644.1:n.1835C>G, NR_121644.1:n.1835C>T

Select item 14884426266.

rs1488442626 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 4:190066846 (GRCh38)
4:190988001 (GRCh37)
Canonical SPDI:: NC_000004.12:190066845:C:G,NC_000004.12:190066845:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.00002/1 (GnomAD)
T=0.00025/6 (TOMMO)
T=0.13145/382 (KOREAN)
HGVS:: NC_000004.12:g.190066846C>G, NC_000004.12:g.190066846C>T, NC_000004.11:g.190988001C>G, NC_000004.11:g.190988001C>T, NW_015495300.1:g.159447C>G, NW_015495300.1:g.159447C>T, NT_167222.1:g.71830C>G, NT_167222.1:g.71830C>T, NW_015495301.1:g.159447C>G, NW_015495301.1:g.159447C>T, NW_003571034.1:g.159776C>G, NW_003571034.1:g.159776C>T, NR_121644.1:n.2345C>G, NR_121644.1:n.2345C>T

Select item 14883017747.

rs1488301774 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:190066020 (GRCh38)
4:190987175 (GRCh37)
Canonical SPDI:: NC_000004.12:190066019:C:A,NC_000004.12:190066019:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.12667/133 (KOREAN)
HGVS:: NC_000004.12:g.190066020C>A, NC_000004.12:g.190066020C>T, NC_000004.11:g.190987175C>A, NC_000004.11:g.190987175C>T, NW_015495300.1:g.158622C>A, NW_015495300.1:g.158622C>T, NT_167222.1:g.71005C>A, NT_167222.1:g.71005C>T, NW_015495301.1:g.158622C>A, NW_015495301.1:g.158622C>T, NW_003571034.1:g.158950C>A, NW_003571034.1:g.158950C>T, NR_121644.1:n.1519C>A, NR_121644.1:n.1519C>T

Select item 14882125998.

rs1488212599 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:190066459 (GRCh38)
4:190987614 (GRCh37)
Canonical SPDI:: NC_000004.12:190066458:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.01568/186 (ALFA)
C=0.05777/58 (KOREAN)
T=0.16667/2 (Korea1K)
HGVS:: NC_000004.12:g.190066459C>T, NC_000004.11:g.190987614C>T, NW_015495300.1:g.159059C>T, NT_167222.1:g.71442C>T, NW_015495301.1:g.159059C>T, NW_003571034.1:g.159389C>T, NR_121644.1:n.1958C>T

Select item 14878592459.

rs1487859245 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 4:190064967 (GRCh38)
4:190986122 (GRCh37)
Canonical SPDI:: NC_000004.12:190064966:T:A,NC_000004.12:190064966:T:C
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.00016/1 (1000Genomes)
HGVS:: NC_000004.12:g.190064967T>A, NC_000004.12:g.190064967T>C, NC_000004.11:g.190986122T>A, NC_000004.11:g.190986122T>C, NW_015495300.1:g.157571T>A, NW_015495300.1:g.157571T>C, NT_167222.1:g.69954T>A, NT_167222.1:g.69954T>C, NW_015495301.1:g.157571T>A, NW_015495301.1:g.157571T>C, NW_003571034.1:g.157897T>A, NW_003571034.1:g.157897T>C, NR_121644.1:n.466T>A, NR_121644.1:n.466T>C

Select item 148724654710.

rs1487246547 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 4:190065646 (GRCh38)
4:190986801 (GRCh37)
Canonical SPDI:: NC_000004.12:190065645:C:G,NC_000004.12:190065645:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00489/51 (ALFA)
T=0.0222/263 (TOMMO)
C=0.5/1 (Siberian)
HGVS:: NC_000004.12:g.190065646C>G, NC_000004.12:g.190065646C>T, NC_000004.11:g.190986801C>G, NC_000004.11:g.190986801C>T, NW_015495300.1:g.158248C>G, NW_015495300.1:g.158248C>T, NT_167222.1:g.70631C>G, NT_167222.1:g.70631C>T, NW_015495301.1:g.158248C>G, NW_015495301.1:g.158248C>T, NW_003571034.1:g.158576C>G, NW_003571034.1:g.158576C>T, NR_121644.1:n.1145C>G, NR_121644.1:n.1145C>T

Select item 148718508411.

rs1487185084 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 4:190065973 (GRCh38)
4:190987128 (GRCh37)
Canonical SPDI:: NC_000004.12:190065972:G:A,NC_000004.12:190065972:G:C,NC_000004.12:190065972:G:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0./0 (SGDP_PRJ)
A=0.00159/21 (TOMMO)
A=0.17099/277 (KOREAN)
HGVS:: NC_000004.12:g.190065973G>A, NC_000004.12:g.190065973G>C, NC_000004.12:g.190065973G>T, NC_000004.11:g.190987128G>A, NC_000004.11:g.190987128G>C, NC_000004.11:g.190987128G>T, NW_015495300.1:g.158575G>A, NW_015495300.1:g.158575G>C, NW_015495300.1:g.158575G>T, NT_167222.1:g.70958G>A, NT_167222.1:g.70958G>C, NT_167222.1:g.70958G>T, NW_015495301.1:g.158575G>A, NW_015495301.1:g.158575G>C, NW_015495301.1:g.158575G>T, NW_003571034.1:g.158903G>A, NW_003571034.1:g.158903G>C, NW_003571034.1:g.158903G>T, NR_121644.1:n.1472G>A, NR_121644.1:n.1472G>C, NR_121644.1:n.1472G>T

Select item 148678142012.

rs1486781420 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:190065959 (GRCh38)
4:190987114 (GRCh37)
Canonical SPDI:: NC_000004.12:190065958:G:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.02698/320 (ALFA)
T=0.00111/18 (TOMMO)
T=0.03314/56 (KOREAN)
HGVS:: NC_000004.12:g.190065959G>T, NC_000004.11:g.190987114G>T, NW_015495300.1:g.158561G>T, NT_167222.1:g.70944G>T, NW_015495301.1:g.158561G>T, NW_003571034.1:g.158889G>T, NR_121644.1:n.1458G>T

Select item 148657208413.

rs1486572084 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:190064564 (GRCh38)
4:190985719 (GRCh37)
Canonical SPDI:: NC_000004.12:190064563:G:A,NC_000004.12:190064563:G:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000102/13 (GnomAD)
A=0.000312/2 (1000Genomes)
HGVS:: NC_000004.12:g.190064564G>A, NC_000004.12:g.190064564G>T, NC_000004.11:g.190985719G>A, NC_000004.11:g.190985719G>T, NW_015495300.1:g.157168G>A, NW_015495300.1:g.157168G>T, NT_167222.1:g.69551G>A, NT_167222.1:g.69551G>T, NW_015495301.1:g.157168G>A, NW_015495301.1:g.157168G>T, NW_003571034.1:g.157494G>A, NW_003571034.1:g.157494G>T, NR_121644.1:n.63G>A, NR_121644.1:n.63G>T

Select item 148654696814.

rs1486546968 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:190065594 (GRCh38)
4:190986749 (GRCh37)
Canonical SPDI:: NC_000004.12:190065593:T:A
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.00017/2 (ALFA)
T=0./0 (SGDP_PRJ)
HGVS:: NC_000004.12:g.190065594T>A, NC_000004.11:g.190986749T>A, NW_015495300.1:g.158196T>A, NT_167222.1:g.70579T>A, NW_015495301.1:g.158196T>A, NW_003571034.1:g.158524T>A, NR_121644.1:n.1093T>A

Select item 148615697915.

rs1486156979 [Homo sapiens]

Variant type:: DEL
Alleles:: AGG>- [Show Flanks]
Chromosome:: 4:190067732 (GRCh38)
4:190988887 (GRCh37)
Canonical SPDI:: NC_000004.12:190067731:AGG:
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000004.12:g.190067732_190067734del, NC_000004.11:g.190988887_190988889del, NW_015495300.1:g.160343_160345del, NT_167222.1:g.72726_72728del, NW_015495301.1:g.160343_160345del, NW_003571034.1:g.160662_160664del, NR_121644.1:n.3231_3233del

Select item 148583952316.

rs1485839523 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:190067041 (GRCh38)
4:190988196 (GRCh37)
Canonical SPDI:: NC_000004.12:190067040:G:C
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00017/2 (ALFA)
HGVS:: NC_000004.12:g.190067041G>C, NC_000004.11:g.190988196G>C, NW_015495300.1:g.159642G>C, NT_167222.1:g.72025G>C, NW_015495301.1:g.159642G>C, NW_003571034.1:g.159971G>C, NR_121644.1:n.2540G>C

Select item 148517405617.

rs1485174056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:190067433 (GRCh38)
4:190988588 (GRCh37)
Canonical SPDI:: NC_000004.12:190067432:C:A,NC_000004.12:190067432:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00018/3 (ALFA)
A=0.00049/9 (TOMMO)
A=0.00156/10 (1000Genomes)
A=0.14345/416 (KOREAN)
HGVS:: NC_000004.12:g.190067433C>A, NC_000004.12:g.190067433C>T, NC_000004.11:g.190988588C>A, NC_000004.11:g.190988588C>T, NW_015495300.1:g.160033C>A, NW_015495300.1:g.160033C>T, NT_167222.1:g.72416C>A, NT_167222.1:g.72416C>T, NW_015495301.1:g.160033C>A, NW_015495301.1:g.160033C>T, NW_003571034.1:g.160363C>A, NW_003571034.1:g.160363C>T, NR_121644.1:n.2932C>A, NR_121644.1:n.2932C>T

Select item 148504502518.

rs1485045025 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:190066354 (GRCh38)
4:190987509 (GRCh37)
Canonical SPDI:: NC_000004.12:190066353:G:A,NC_000004.12:190066353:G:C
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.03175/12 (KOREAN)
HGVS:: NC_000004.12:g.190066354G>A, NC_000004.12:g.190066354G>C, NC_000004.11:g.190987509G>A, NC_000004.11:g.190987509G>C, NW_015495300.1:g.158956G>A, NW_015495300.1:g.158956G>C, NT_167222.1:g.71339G>A, NT_167222.1:g.71339G>C, NW_015495301.1:g.158956G>A, NW_015495301.1:g.158956G>C, NW_003571034.1:g.159284G>A, NW_003571034.1:g.159284G>C, NR_121644.1:n.1853G>A, NR_121644.1:n.1853G>C

Select item 148495259219.

rs1484952592 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:190067207 (GRCh38)
4:190988362 (GRCh37)
Canonical SPDI:: NC_000004.12:190067206:G:A,NC_000004.12:190067206:G:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00063/8 (TOMMO)
A=0.0069/2 (Korea1K)
A=0.12706/370 (KOREAN)
HGVS:: NC_000004.12:g.190067207G>A, NC_000004.12:g.190067207G>T, NC_000004.11:g.190988362G>A, NC_000004.11:g.190988362G>T, NW_015495300.1:g.159808G>A, NW_015495300.1:g.159808G>T, NT_167222.1:g.72191G>A, NT_167222.1:g.72191G>T, NW_015495301.1:g.159808G>A, NW_015495301.1:g.159808G>T, NW_003571034.1:g.160137G>A, NW_003571034.1:g.160137G>T, NR_121644.1:n.2706G>A, NR_121644.1:n.2706G>T

Select item 148485820120.

rs1484858201 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:190066754 (GRCh38)
4:190987909 (GRCh37)
Canonical SPDI:: NC_000004.12:190066753:C:T
Gene:: DBET (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.00008/1 (ALFA)
T=0.00027/18 (GnomAD)
HGVS:: NC_000004.12:g.190066754C>T, NC_000004.11:g.190987909C>T, NW_015495300.1:g.159355C>T, NT_167222.1:g.71738C>T, NW_015495301.1:g.159355C>T, NW_003571034.1:g.159684C>T, NR_121644.1:n.2253C>T

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