SNP Links for Nucleotide (Select 302393556) - SNP

Links from Nucleotide

Items: 1 to 20 of 79

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Select item 14692197251.

rs1469219725 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:110937436 (GRCh38)
12:111375240 (GRCh37)
Canonical SPDI:: NC_000012.12:110937435:T:C
Gene:: LINC01405 (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_000012.12:g.110937436T>C, NC_000012.11:g.111375240T>C, NG_079817.1:g.372T>C, NR_036513.1:n.349T>C

Select item 14657017042.

rs1465701704 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:110937338 (GRCh38)
12:111375142 (GRCh37)
Canonical SPDI:: NC_000012.12:110937337:C:T
Gene:: LINC01405 (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.110937338C>T, NC_000012.11:g.111375142C>T, NG_079817.1:g.274C>T, NR_036513.1:n.251C>T

Select item 14583041663.

rs1458304166 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 12:110936692 (GRCh38)
12:111374496 (GRCh37)
Canonical SPDI:: NC_000012.12:110936691:C:A,NC_000012.12:110936691:C:T
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.110936692C>A, NC_000012.12:g.110936692C>T, NC_000012.11:g.111374496C>A, NC_000012.11:g.111374496C>T, NR_036513.1:n.91C>A, NR_036513.1:n.91C>T

Select item 14575389194.

rs1457538919 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:110937218 (GRCh38)
12:111375022 (GRCh37)
Canonical SPDI:: NC_000012.12:110937217:C:T
Gene:: LINC01405 (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_000012.12:g.110937218C>T, NC_000012.11:g.111375022C>T, NG_079817.1:g.154C>T, NR_036513.1:n.131C>T

Select item 14507663105.

rs1450766310 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:110937306 (GRCh38)
12:111375110 (GRCh37)
Canonical SPDI:: NC_000012.12:110937305:C:T
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.110937306C>T, NC_000012.11:g.111375110C>T, NG_079817.1:g.242C>T, NR_036513.1:n.219C>T

Select item 14442281256.

rs1444228125 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:110936666 (GRCh38)
12:111374470 (GRCh37)
Canonical SPDI:: NC_000012.12:110936665:C:T
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000012.12:g.110936666C>T, NC_000012.11:g.111374470C>T, NR_036513.1:n.65C>T

Select item 14366601157.

rs1436660115 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:110937258 (GRCh38)
12:111375062 (GRCh37)
Canonical SPDI:: NC_000012.12:110937257:G:A
Gene:: LINC01405 (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_000012.12:g.110937258G>A, NC_000012.11:g.111375062G>A, NG_079817.1:g.194G>A, NR_036513.1:n.171G>A

Select item 14272779488.

rs1427277948 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 12:110936648 (GRCh38)
12:111374452 (GRCh37)
Canonical SPDI:: NC_000012.12:110936645:GTGT:GT
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GTGT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.110936646GT[1], NC_000012.11:g.111374450GT[1], NR_036513.1:n.45GT[1]

Select item 14236947739.

rs1423694773 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 12:110937248 (GRCh38)
12:111375052 (GRCh37)
Canonical SPDI:: NC_000012.12:110937247:G:T
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000029/4 (GnomAD)
T=0.000049/13 (TOPMED)
T=0.001062/18 (TOMMO)
T=0.001711/5 (KOREAN)
HGVS:: NC_000012.12:g.110937248G>T, NC_000012.11:g.111375052G>T, NG_079817.1:g.184G>T, NR_036513.1:n.161G>T

Select item 141633184010.

rs1416331840 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 12:110936647 (GRCh38)
12:111374451 (GRCh37)
Canonical SPDI:: NC_000012.12:110936646:T:C,NC_000012.12:110936646:T:G
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.110936647T>C, NC_000012.12:g.110936647T>G, NC_000012.11:g.111374451T>C, NC_000012.11:g.111374451T>G, NR_036513.1:n.46T>C, NR_036513.1:n.46T>G

Select item 140671722911.

rs1406717229 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 12:110937403 (GRCh38)
12:111375208 (GRCh37)
Canonical SPDI:: NC_000012.12:110937403:AAAA:AAAAA
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.110937407dup, NC_000012.11:g.111375211dup, NG_079817.1:g.343dup, NR_036513.1:n.320dup

Select item 140326640212.

rs1403266402 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:110937203 (GRCh38)
12:111375007 (GRCh37)
Canonical SPDI:: NC_000012.12:110937202:T:C
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.110937203T>C, NC_000012.11:g.111375007T>C, NG_079817.1:g.139T>C, NR_036513.1:n.116T>C

Select item 140162651913.

rs1401626519 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:110936634 (GRCh38)
12:111374438 (GRCh37)
Canonical SPDI:: NC_000012.12:110936633:C:T
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.110936634C>T, NC_000012.11:g.111374438C>T, NR_036513.1:n.33C>T

Select item 139794112614.

rs1397941126 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 12:110937201 (GRCh38)
12:111375005 (GRCh37)
Canonical SPDI:: NC_000012.12:110937200:T:A
Gene:: LINC01405 (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.110937201T>A, NC_000012.11:g.111375005T>A, NG_079817.1:g.137T>A, NR_036513.1:n.114T>A

Select item 139575709915.

rs1395757099 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:110937325 (GRCh38)
12:111375129 (GRCh37)
Canonical SPDI:: NC_000012.12:110937324:A:G
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.110937325A>G, NC_000012.11:g.111375129A>G, NG_079817.1:g.261A>G, NR_036513.1:n.238A>G

Select item 138377342516.

rs1383773425 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:110937294 (GRCh38)
12:111375098 (GRCh37)
Canonical SPDI:: NC_000012.12:110937293:C:G
Gene:: LINC01405 (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.110937294C>G, NC_000012.11:g.111375098C>G, NG_079817.1:g.230C>G, NR_036513.1:n.207C>G

Select item 137018808517.

rs1370188085 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:110936615 (GRCh38)
12:111374419 (GRCh37)
Canonical SPDI:: NC_000012.12:110936614:G:A
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.110936615G>A, NC_000012.11:g.111374419G>A, NR_036513.1:n.14G>A

Select item 134338474718.

rs1343384747 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:110936637 (GRCh38)
12:111374441 (GRCh37)
Canonical SPDI:: NC_000012.12:110936636:C:G
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.110936637C>G, NC_000012.11:g.111374441C>G, NR_036513.1:n.36C>G

Select item 133615105319.

rs1336151053 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 12:110937204 (GRCh38)
12:111375008 (GRCh37)
Canonical SPDI:: NC_000012.12:110937203:A:T
Gene:: LINC01405 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000012.12:g.110937204A>T, NC_000012.11:g.111375008A>T, NG_079817.1:g.140A>T, NR_036513.1:n.117A>T

Select item 133506171220.

rs1335061712 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:110937384 (GRCh38)
12:111375188 (GRCh37)
Canonical SPDI:: NC_000012.12:110937383:C:T
Gene:: LINC01405 (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_000012.12:g.110937384C>T, NC_000012.11:g.111375188C>T, NG_079817.1:g.320C>T, NR_036513.1:n.297C>T

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Links from Nucleotide

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