SNP Links for Nucleotide (Select 635574638) - SNP

Links from Nucleotide

Items: 1 to 20 of 121

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Select item 14858179801.

rs1485817980 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:108459485 (GRCh38)
12:108853262 (GRCh37)
Canonical SPDI:: NC_000012.12:108459484:C:A
Gene:: LINC01498 (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_000012.12:g.108459485C>A, NC_000012.11:g.108853262C>A, NR_120483.1:n.489G>T

Select item 14721561362.

rs1472156136 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:108459572 (GRCh38)
12:108853349 (GRCh37)
Canonical SPDI:: NC_000012.12:108459571:A:G
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.108459572A>G, NC_000012.11:g.108853349A>G, NR_120483.1:n.402T>C

Select item 14668939403.

rs1466893940 [Homo sapiens]

Variant type:: DELINS
Alleles:: ATAA>- [Show Flanks]
Chromosome:: 12:108473615 (GRCh38)
12:108867392 (GRCh37)
Canonical SPDI:: NC_000012.12:108473612:AAATAA:AA
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.108473615_108473618del, NC_000012.11:g.108867392_108867395del, NR_120483.1:n.74_77del

Select item 14668304334.

rs1466830433 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:108473041 (GRCh38)
12:108866818 (GRCh37)
Canonical SPDI:: NC_000012.12:108473040:C:T
Gene:: LINC01498 (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=0.000029/4 (GnomAD)
HGVS:: NC_000012.12:g.108473041C>T, NC_000012.11:g.108866818C>T, NR_120483.1:n.285G>A

Select item 14663311155.

rs1466331115 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:108461631 (GRCh38)
12:108855408 (GRCh37)
Canonical SPDI:: NC_000012.12:108461630:A:G
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000012.12:g.108461631A>G, NC_000012.11:g.108855408A>G, NR_120483.1:n.388T>C

Select item 14605945526.

rs1460594552 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:108461677 (GRCh38)
12:108855454 (GRCh37)
Canonical SPDI:: NC_000012.12:108461676:G:A
Gene:: LINC01498 (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_000012.12:g.108461677G>A, NC_000012.11:g.108855454G>A, NR_120483.1:n.342C>T

Select item 14561080667.

rs1456108066 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 12:108473173 (GRCh38)
12:108866950 (GRCh37)
Canonical SPDI:: NC_000012.12:108473172:G:T
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000023/6 (TOPMED)
HGVS:: NC_000012.12:g.108473173G>T, NC_000012.11:g.108866950G>T, NR_120483.1:n.153C>A

Select item 14458769098.

rs1445876909 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 12:108459442 (GRCh38)
12:108853219 (GRCh37)
Canonical SPDI:: NC_000012.12:108459441:A:T
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.108459442A>T, NC_000012.11:g.108853219A>T, NR_120483.1:n.532T>A

Select item 14413513129.

rs1441351312 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:108459437 (GRCh38)
12:108853214 (GRCh37)
Canonical SPDI:: NC_000012.12:108459436:T:C
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000012.12:g.108459437T>C, NC_000012.11:g.108853214T>C, NR_120483.1:n.537A>G

Select item 144108034510.

rs1441080345 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:108473601 (GRCh38)
12:108867378 (GRCh37)
Canonical SPDI:: NC_000012.12:108473600:T:C
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000012.12:g.108473601T>C, NC_000012.11:g.108867378T>C, NR_120483.1:n.89A>G

Select item 143301634811.

rs1433016348 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:108473051 (GRCh38)
12:108866828 (GRCh37)
Canonical SPDI:: NC_000012.12:108473050:A:G
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.108473051A>G, NC_000012.11:g.108866828A>G, NR_120483.1:n.275T>C

Select item 141794825612.

rs1417948256 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:108473011 (GRCh38)
12:108866788 (GRCh37)
Canonical SPDI:: NC_000012.12:108473010:G:A
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.108473011G>A, NC_000012.11:g.108866788G>A, NR_120483.1:n.315C>T

Select item 141558743513.

rs1415587435 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:108459541 (GRCh38)
12:108853318 (GRCh37)
Canonical SPDI:: NC_000012.12:108459540:C:G
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000012.12:g.108459541C>G, NC_000012.11:g.108853318C>G, NR_120483.1:n.433G>C

Select item 141498209614.

rs1414982096 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:108459579 (GRCh38)
12:108853356 (GRCh37)
Canonical SPDI:: NC_000012.12:108459578:A:G
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.108459579A>G, NC_000012.11:g.108853356A>G, NR_120483.1:n.395T>C

Select item 140281552215.

rs1402815522 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:108459558 (GRCh38)
12:108853335 (GRCh37)
Canonical SPDI:: NC_000012.12:108459557:T:C
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.108459558T>C, NC_000012.11:g.108853335T>C, NR_120483.1:n.416A>G

Select item 139407084616.

rs1394070846 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>-,GG [Show Flanks]
Chromosome:: 12:108461645 (GRCh38)
12:108855422 (GRCh37)
Canonical SPDI:: NC_000012.12:108461644:GGGGGG:GGGGG,NC_000012.12:108461644:GGGGGG:GGGGGGG
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGGGGG=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.108461650del, NC_000012.12:g.108461650dup, NC_000012.11:g.108855427del, NC_000012.11:g.108855427dup, NR_120483.1:n.374del, NR_120483.1:n.374dup

Select item 138838386817.

rs1388383868 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:108473093 (GRCh38)
12:108866870 (GRCh37)
Canonical SPDI:: NC_000012.12:108473092:A:G
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_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_000012.12:g.108473093A>G, NC_000012.11:g.108866870A>G, NR_120483.1:n.233T>C

Select item 138814221018.

rs1388142210 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 12:108461679 (GRCh38)
12:108855456 (GRCh37)
Canonical SPDI:: NC_000012.12:108461678:A:C,NC_000012.12:108461678:A:T
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000012.12:g.108461679A>C, NC_000012.12:g.108461679A>T, NC_000012.11:g.108855456A>C, NC_000012.11:g.108855456A>T, NR_120483.1:n.340T>G, NR_120483.1:n.340T>A

Select item 138624353019.

rs1386243530 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 12:108459562 (GRCh38)
12:108853339 (GRCh37)
Canonical SPDI:: NC_000012.12:108459561:G:C,NC_000012.12:108459561:G:T
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.108459562G>C, NC_000012.12:g.108459562G>T, NC_000012.11:g.108853339G>C, NC_000012.11:g.108853339G>T, NR_120483.1:n.412C>G, NR_120483.1:n.412C>A

Select item 137935480820.

rs1379354808 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:108473635 (GRCh38)
12:108867412 (GRCh37)
Canonical SPDI:: NC_000012.12:108473634:A:G
Gene:: LINC01498 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.108473635A>G, NC_000012.11:g.108867412A>G, NR_120483.1:n.55T>C

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