SNP Links for Nucleotide (Select 224028264) - SNP

Links from Nucleotide

Items: 1 to 20 of 269

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Select item 14896365841.

rs1489636584 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:133088336 (GRCh38)
6:133409475 (GRCh37)
Canonical SPDI:: NC_000006.12:133088335:G:A
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000006.12:g.133088336G>A, NC_000006.11:g.133409475G>A, NR_026969.1:n.257G>A

Select item 14838916372.

rs1483891637 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:133096546 (GRCh38)
6:133417685 (GRCh37)
Canonical SPDI:: NC_000006.12:133096545:C:A
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.133096546C>A, NC_000006.11:g.133417685C>A, NR_026969.1:n.535C>A

Select item 14822145643.

rs1482214564 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:133088405 (GRCh38)
6:133409544 (GRCh37)
Canonical SPDI:: NC_000006.12:133088404:A:G
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.133088405A>G, NC_000006.11:g.133409544A>G, NR_026969.1:n.326A>G

Select item 14818543904.

rs1481854390 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:133088277 (GRCh38)
6:133409416 (GRCh37)
Canonical SPDI:: NC_000006.12:133088276:C:A
Gene:: LINC00326 (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=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.133088277C>A, NC_000006.11:g.133409416C>A, NR_026969.1:n.198C>A

Select item 14813432015.

rs1481343201 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:133106536 (GRCh38)
6:133427675 (GRCh37)
Canonical SPDI:: NC_000006.12:133106535:C:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.133106536C>T, NC_000006.11:g.133427675C>T, NR_026969.1:n.1172C>T

Select item 14797262816.

rs1479726281 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:133106514 (GRCh38)
6:133427653 (GRCh37)
Canonical SPDI:: NC_000006.12:133106513:C:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.133106514C>T, NC_000006.11:g.133427653C>T, NR_026969.1:n.1150C>T

Select item 14751476037.

rs1475147603 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:133106434 (GRCh38)
6:133427573 (GRCh37)
Canonical SPDI:: NC_000006.12:133106433:C:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.133106434C>T, NC_000006.11:g.133427573C>T, NR_026969.1:n.1070C>T

Select item 14741305488.

rs1474130548 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:133106162 (GRCh38)
6:133427301 (GRCh37)
Canonical SPDI:: NC_000006.12:133106161:A:G
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_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_000006.12:g.133106162A>G, NC_000006.11:g.133427301A>G, NR_026969.1:n.798A>G, NM_001037231.1:c.153A>G

Select item 14740175839.

rs1474017583 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:133106359 (GRCh38)
6:133427498 (GRCh37)
Canonical SPDI:: NC_000006.12:133106358:T:A
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000006.12:g.133106359T>A, NC_000006.11:g.133427498T>A, NR_026969.1:n.995T>A

Select item 146932747910.

rs1469327479 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:133088274 (GRCh38)
6:133409413 (GRCh37)
Canonical SPDI:: NC_000006.12:133088273:C:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.133088274C>T, NC_000006.11:g.133409413C>T, NR_026969.1:n.195C>T

Select item 146875118611.

rs1468751186 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:133106288 (GRCh38)
6:133427427 (GRCh37)
Canonical SPDI:: NC_000006.12:133106287:C:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000342/1 (KOREAN)
HGVS:: NC_000006.12:g.133106288C>T, NC_000006.11:g.133427427C>T, NR_026969.1:n.924C>T, NM_001037231.1:c.279C>T

Select item 146068206112.

rs1460682061 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTAAGACAAGGT>- [Show Flanks]
Chromosome:: 6:133096554 (GRCh38)
6:133417693 (GRCh37)
Canonical SPDI:: NC_000006.12:133096551:GTTTAAGACAAGGT:GT
Gene:: LINC00326 (Varview)
Functional Consequence:: splice_donor_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GT=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.133096554_133096565del, NC_000006.11:g.133417693_133417704del

Select item 145828442013.

rs1458284420 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 6:133088395 (GRCh38)
6:133409534 (GRCh37)
Canonical SPDI:: NC_000006.12:133088394:C:G,NC_000006.12:133088394:C:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.133088395C>G, NC_000006.12:g.133088395C>T, NC_000006.11:g.133409534C>G, NC_000006.11:g.133409534C>T, NR_026969.1:n.316C>G, NR_026969.1:n.316C>T

Select item 145587875814.

rs1455878758 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:133100128 (GRCh38)
6:133421267 (GRCh37)
Canonical SPDI:: NC_000006.12:133100127:A:G
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.133100128A>G, NC_000006.11:g.133421267A>G, NR_026969.1:n.674A>G, NM_001037231.1:c.29A>G

Select item 145209686615.

rs1452096866 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 6:133096541 (GRCh38)
6:133417680 (GRCh37)
Canonical SPDI:: NC_000006.12:133096540:A:G,NC_000006.12:133096540:A:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.133096541A>G, NC_000006.12:g.133096541A>T, NC_000006.11:g.133417680A>G, NC_000006.11:g.133417680A>T, NR_026969.1:n.530A>G, NR_026969.1:n.530A>T

Select item 145124590216.

rs1451245902 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:133106347 (GRCh38)
6:133427486 (GRCh37)
Canonical SPDI:: NC_000006.12:133106346:G:A,NC_000006.12:133106346:G:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000036/5 (GnomAD)
HGVS:: NC_000006.12:g.133106347G>A, NC_000006.12:g.133106347G>T, NC_000006.11:g.133427486G>A, NC_000006.11:g.133427486G>T, NR_026969.1:n.983G>A, NR_026969.1:n.983G>T

Select item 144834097317.

rs1448340973 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 6:133088265 (GRCh38)
6:133409404 (GRCh37)
Canonical SPDI:: NC_000006.12:133088264:T:A,NC_000006.12:133088264:T:C
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.133088265T>A, NC_000006.12:g.133088265T>C, NC_000006.11:g.133409404T>A, NC_000006.11:g.133409404T>C, NR_026969.1:n.186T>A, NR_026969.1:n.186T>C

Select item 144790876318.

rs1447908763 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:133096519 (GRCh38)
6:133417658 (GRCh37)
Canonical SPDI:: NC_000006.12:133096518:C:A
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000006.12:g.133096519C>A, NC_000006.11:g.133417658C>A, NR_026969.1:n.508C>A

Select item 144665004819.

rs1446650048 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:133100080 (GRCh38)
6:133421219 (GRCh37)
Canonical SPDI:: NC_000006.12:133100079:T:A
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.0002/1 (ALFA)
A=0.0002/1 (Estonian)
HGVS:: NC_000006.12:g.133100080T>A, NC_000006.11:g.133421219T>A, NR_026969.1:n.626T>A, NM_001037231.1:c.-20T>A

Select item 144301809120.

rs1443018091 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:133088220 (GRCh38)
6:133409359 (GRCh37)
Canonical SPDI:: NC_000006.12:133088219:C:T
Gene:: LINC00326 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.133088220C>T, NC_000006.11:g.133409359C>T, NR_026969.1:n.141C>T

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