SNP Links for Nucleotide (Select 570700909) - SNP

Links from Nucleotide

Items: 1 to 20 of 261

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Select item 14908930131.

rs1490893013 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 12:42615627 (GRCh38)
12:43009429 (GRCh37)
Canonical SPDI:: NC_000012.12:42615626:G:T
Gene:: LINC02402 (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)
HGVS:: NC_000012.12:g.42615627G>T, NC_000012.11:g.43009429G>T, NR_110042.1:n.1088C>A

Select item 14887281392.

rs1488728139 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:42629617 (GRCh38)
12:43023419 (GRCh37)
Canonical SPDI:: NC_000012.12:42629616:C:T
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/2 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000012.12:g.42629617C>T, NC_000012.11:g.43023419C>T, NR_110042.1:n.596G>A

Select item 14886666423.

rs1488666642 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:42615522 (GRCh38)
12:43009324 (GRCh37)
Canonical SPDI:: NC_000012.12:42615521:T:G
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000012.12:g.42615522T>G, NC_000012.11:g.43009324T>G, NR_110042.1:n.1193A>C

Select item 14849138534.

rs1484913853 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 12:42643368 (GRCh38)
12:43037170 (GRCh37)
Canonical SPDI:: NC_000012.12:42643367:T:A,NC_000012.12:42643367:T:C
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.42643368T>A, NC_000012.12:g.42643368T>C, NC_000012.11:g.43037170T>A, NC_000012.11:g.43037170T>C, NR_110042.1:n.354A>T, NR_110042.1:n.354A>G

Select item 14842292845.

rs1484229284 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:42615939 (GRCh38)
12:43009741 (GRCh37)
Canonical SPDI:: NC_000012.12:42615938:G:A
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.42615939G>A, NC_000012.11:g.43009741G>A, NR_110042.1:n.776C>T

Select item 14842262126.

rs1484226212 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:42644242 (GRCh38)
12:43038044 (GRCh37)
Canonical SPDI:: NC_000012.12:42644241:T:C
Gene:: LINC02402 (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.42644242T>C, NC_000012.11:g.43038044T>C, NR_110042.1:n.282A>G

Select item 14819000867.

rs1481900086 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:42646324 (GRCh38)
12:43040126 (GRCh37)
Canonical SPDI:: NC_000012.12:42646323:G:A
Gene:: LINC02402 (Varview), LINC02451 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.42646324G>A, NC_000012.11:g.43040126G>A, NR_110042.1:n.175C>T

Select item 14787106188.

rs1478710618 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 12:42634367 (GRCh38)
12:43028169 (GRCh37)
Canonical SPDI:: NC_000012.12:42634366:A:C,NC_000012.12:42634366:A:G
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.42634367A>C, NC_000012.12:g.42634367A>G, NC_000012.11:g.43028169A>C, NC_000012.11:g.43028169A>G, NR_110042.1:n.440T>G, NR_110042.1:n.440T>C

Select item 14784742759.

rs1478474275 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:42615606 (GRCh38)
12:43009408 (GRCh37)
Canonical SPDI:: NC_000012.12:42615605:A:G
Gene:: LINC02402 (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.42615606A>G, NC_000012.11:g.43009408A>G, NR_110042.1:n.1109T>C

Select item 147470304110.

rs1474703041 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:42643350 (GRCh38)
12:43037152 (GRCh37)
Canonical SPDI:: NC_000012.12:42643349:C:T
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.42643350C>T, NC_000012.11:g.43037152C>T, NR_110042.1:n.372G>A

Select item 147462467311.

rs1474624673 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:42646476 (GRCh38)
12:43040278 (GRCh37)
Canonical SPDI:: NC_000012.12:42646475:T:C
Gene:: LINC02402 (Varview), LINC02451 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,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.42646476T>C, NC_000012.11:g.43040278T>C, NR_110042.1:n.23A>G

Select item 147333156312.

rs1473331563 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:42643344 (GRCh38)
12:43037146 (GRCh37)
Canonical SPDI:: NC_000012.12:42643343:A:G
Gene:: LINC02402 (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_000012.12:g.42643344A>G, NC_000012.11:g.43037146A>G, NR_110042.1:n.378T>C

Select item 147039704213.

rs1470397042 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:42629547 (GRCh38)
12:43023349 (GRCh37)
Canonical SPDI:: NC_000012.12:42629546:C:T
Gene:: LINC02402 (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=0.000073/1 (TOMMO)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000012.12:g.42629547C>T, NC_000012.11:g.43023349C>T, NR_110042.1:n.666G>A

Select item 146758802314.

rs1467588023 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:42615876 (GRCh38)
12:43009678 (GRCh37)
Canonical SPDI:: NC_000012.12:42615875:T:C
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000012.12:g.42615876T>C, NC_000012.11:g.43009678T>C, NR_110042.1:n.839A>G

Select item 146657991915.

rs1466579919 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:42615735 (GRCh38)
12:43009537 (GRCh37)
Canonical SPDI:: NC_000012.12:42615734:A:G
Gene:: LINC02402 (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.42615735A>G, NC_000012.11:g.43009537A>G, NR_110042.1:n.980T>C

Select item 146262771816.

rs1462627718 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 12:42629566 (GRCh38)
12:43023368 (GRCh37)
Canonical SPDI:: NC_000012.12:42629565:A:C
Gene:: LINC02402 (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_000012.12:g.42629566A>C, NC_000012.11:g.43023368A>C, NR_110042.1:n.647T>G

Select item 146161852817.

rs1461618528 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:42615718 (GRCh38)
12:43009520 (GRCh37)
Canonical SPDI:: NC_000012.12:42615717:C:G
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000012.12:g.42615718C>G, NC_000012.11:g.43009520C>G, NR_110042.1:n.997G>C

Select item 145838080118.

rs1458380801 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:42643407 (GRCh38)
12:43037209 (GRCh37)
Canonical SPDI:: NC_000012.12:42643406:C:T
Gene:: LINC02402 (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.42643407C>T, NC_000012.11:g.43037209C>T, NR_110042.1:n.315G>A

Select item 145642219719.

rs1456422197 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:42629466 (GRCh38)
12:43023268 (GRCh37)
Canonical SPDI:: NC_000012.12:42629465:C:T
Gene:: LINC02402 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.42629466C>T, NC_000012.11:g.43023268C>T, NR_110042.1:n.747G>A

Select item 145502680220.

rs1455026802 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:42629623 (GRCh38)
12:43023425 (GRCh37)
Canonical SPDI:: NC_000012.12:42629622:T:G
Gene:: LINC02402 (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_000012.12:g.42629623T>G, NC_000012.11:g.43023425T>G, NR_110042.1:n.590A>C

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