SNP Links for Nucleotide (Select 634743336) - SNP

Links from Nucleotide

Items: 1 to 20 of 167

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Select item 14883685251.

rs1488368525 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:27236722 (GRCh38)
13:27810859 (GRCh37)
Canonical SPDI:: NC_000013.11:27236721:T:C
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000013.11:g.27236722T>C, NC_000013.10:g.27810859T>C, NR_120429.1:n.536A>G

Select item 14878970872.

rs1487897087 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:27237080 (GRCh38)
13:27811217 (GRCh37)
Canonical SPDI:: NC_000013.11:27237079:G:A
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.27237080G>A, NC_000013.10:g.27811217G>A, NR_120429.1:n.178C>T

Select item 14833185693.

rs1483318569 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:27236784 (GRCh38)
13:27810921 (GRCh37)
Canonical SPDI:: NC_000013.11:27236783:G:C
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.27236784G>C, NC_000013.10:g.27810921G>C, NR_120429.1:n.474C>G

Select item 14737674414.

rs1473767441 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:27236566 (GRCh38)
13:27810703 (GRCh37)
Canonical SPDI:: NC_000013.11:27236565:T:G
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.27236566T>G, NC_000013.10:g.27810703T>G, NR_120429.1:n.582A>C

Select item 14719041875.

rs1471904187 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 13:27237146 (GRCh38)
13:27811283 (GRCh37)
Canonical SPDI:: NC_000013.11:27237145:G:C,NC_000013.11:27237145:G:T
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.27237146G>C, NC_000013.11:g.27237146G>T, NC_000013.10:g.27811283G>C, NC_000013.10:g.27811283G>T, NR_120429.1:n.112C>G, NR_120429.1:n.112C>A

Select item 14707044276.

rs1470704427 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:27236801 (GRCh38)
13:27810938 (GRCh37)
Canonical SPDI:: NC_000013.11:27236800:A:G
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.27236801A>G, NC_000013.10:g.27810938A>G, NR_120429.1:n.457T>C

Select item 14636834767.

rs1463683476 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:27236538 (GRCh38)
13:27810675 (GRCh37)
Canonical SPDI:: NC_000013.11:27236537:A:G
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.27236538A>G, NC_000013.10:g.27810675A>G, NR_120429.1:n.610T>C

Select item 14562542468.

rs1456254246 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 13:27236330 (GRCh38)
13:27810467 (GRCh37)
Canonical SPDI:: NC_000013.11:27236329:C:A
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.27236330C>A, NC_000013.10:g.27810467C>A, NR_120429.1:n.818G>T

Select item 14541906369.

rs1454190636 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:27236930 (GRCh38)
13:27811067 (GRCh37)
Canonical SPDI:: NC_000013.11:27236929:T:G
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.27236930T>G, NC_000013.10:g.27811067T>G, NR_120429.1:n.328A>C

Select item 145405209310.

rs1454052093 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:27236360 (GRCh38)
13:27810497 (GRCh37)
Canonical SPDI:: NC_000013.11:27236359:T:G
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000076/20 (TOPMED)
HGVS:: NC_000013.11:g.27236360T>G, NC_000013.10:g.27810497T>G, NR_120429.1:n.788A>C

Select item 144659464411.

rs1446594644 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:27236362 (GRCh38)
13:27810499 (GRCh37)
Canonical SPDI:: NC_000013.11:27236361:T:C
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.27236362T>C, NC_000013.10:g.27810499T>C, NR_120429.1:n.786A>G

Select item 144077476312.

rs1440774763 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:27237066 (GRCh38)
13:27811203 (GRCh37)
Canonical SPDI:: NC_000013.11:27237065:T:C
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.27237066T>C, NC_000013.10:g.27811203T>C, NR_120429.1:n.192A>G

Select item 143456581213.

rs1434565812 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTTA>- [Show Flanks]
Chromosome:: 13:27237097 (GRCh38)
13:27811234 (GRCh37)
Canonical SPDI:: NC_000013.11:27237093:TTACTTA:TTA
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.27237097_27237100del, NC_000013.10:g.27811234_27811237del, NR_120429.1:n.161_164del

Select item 143306715114.

rs1433067151 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:27236553 (GRCh38)
13:27810690 (GRCh37)
Canonical SPDI:: NC_000013.11:27236552:C:T
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.27236553C>T, NC_000013.10:g.27810690C>T, NR_120429.1:n.595G>A

Select item 142676745915.

rs1426767459 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:27236833 (GRCh38)
13:27810970 (GRCh37)
Canonical SPDI:: NC_000013.11:27236832:G:A
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.27236833G>A, NC_000013.10:g.27810970G>A, NR_120429.1:n.425C>T

Select item 142150517016.

rs1421505170 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 13:27237257 (GRCh38)
13:27811394 (GRCh37)
Canonical SPDI:: NC_000013.11:27237256:T:A
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.27237257T>A, NC_000013.10:g.27811394T>A, NR_120429.1:n.1A>T

Select item 141771645917.

rs1417716459 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 13:27236581 (GRCh38)
13:27810718 (GRCh37)
Canonical SPDI:: NC_000013.11:27236580:C:A,NC_000013.11:27236580:C:T
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.27236581C>A, NC_000013.11:g.27236581C>T, NC_000013.10:g.27810718C>A, NC_000013.10:g.27810718C>T, NR_120429.1:n.567G>T, NR_120429.1:n.567G>A

Select item 141289472018.

rs1412894720 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:27236575 (GRCh38)
13:27810712 (GRCh37)
Canonical SPDI:: NC_000013.11:27236574:G:A
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.27236575G>A, NC_000013.10:g.27810712G>A, NR_120429.1:n.573C>T

Select item 141219425319.

rs1412194253 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:27236759 (GRCh38)
13:27810896 (GRCh37)
Canonical SPDI:: NC_000013.11:27236758:A:C
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
HGVS:: NC_000013.11:g.27236759A>C, NC_000013.10:g.27810896A>C, NR_120429.1:n.499T>G

Select item 141094988220.

rs1410949882 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:27236885 (GRCh38)
13:27811022 (GRCh37)
Canonical SPDI:: NC_000013.11:27236884:G:A
Gene:: LINC00412 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.27236885G>A, NC_000013.10:g.27811022G>A, NR_120429.1:n.373C>T

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