SNP Links for Nucleotide (Select 570700904) - SNP

Links from Nucleotide

Items: 1 to 20 of 450

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Select item 14901115021.

rs1490111502 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:113745254 (GRCh38)
12:114183059 (GRCh37)
Canonical SPDI:: NC_000012.12:113745253:T:C
Gene:: LINC01234 (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.113745254T>C, NC_000012.11:g.114183059T>C, NR_110026.1:n.1545A>G, NR_110025.1:n.1411A>G

Select item 14897762202.

rs1489776220 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:113745941 (GRCh38)
12:114183746 (GRCh37)
Canonical SPDI:: NC_000012.12:113745940:C:T
Gene:: LINC01234 (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.113745941C>T, NC_000012.11:g.114183746C>T, NR_110026.1:n.858G>A, NR_110025.1:n.724G>A

Select item 14877527913.

rs1487752791 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:113744949 (GRCh38)
12:114182754 (GRCh37)
Canonical SPDI:: NC_000012.12:113744948:G:A
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000036/5 (GnomAD)
HGVS:: NC_000012.12:g.113744949G>A, NC_000012.11:g.114182754G>A, NR_110026.1:n.1850C>T, NR_110025.1:n.1716C>T

Select item 14840507654.

rs1484050765 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 12:113745006 (GRCh38)
12:114182811 (GRCh37)
Canonical SPDI:: NC_000012.12:113745005:G:
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.113745006del, NC_000012.11:g.114182811del, NR_110026.1:n.1793del, NR_110025.1:n.1659del

Select item 14832271645.

rs1483227164 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 12:113746388 (GRCh38)
12:114184193 (GRCh37)
Canonical SPDI:: NC_000012.12:113746387:CCC:CC
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0.000071/1 (ALFA)
-=0.000023/6 (TOPMED)
-=0.000029/4 (GnomAD)
HGVS:: NC_000012.12:g.113746390del, NC_000012.11:g.114184195del, NR_110026.1:n.411del, NR_110025.1:n.277del

Select item 14820818426.

rs1482081842 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:113745609 (GRCh38)
12:114183414 (GRCh37)
Canonical SPDI:: NC_000012.12:113745608:C:T
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000026/7 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000012.12:g.113745609C>T, NC_000012.11:g.114183414C>T, NR_110026.1:n.1190G>A, NR_110025.1:n.1056G>A

Select item 14795748517.

rs1479574851 [Homo sapiens]

Variant type:: DELINS
Alleles:: GACT>- [Show Flanks]
Chromosome:: 12:113745939 (GRCh38)
12:114183744 (GRCh37)
Canonical SPDI:: NC_000012.12:113745935:ACTGACT:ACT
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACT=0./0 (ALFA)
-=0.000021/3 (GnomAD)
-=0.000034/9 (TOPMED)
HGVS:: NC_000012.12:g.113745939_113745942del, NC_000012.11:g.114183744_114183747del, NR_110026.1:n.860_863del, NR_110025.1:n.726_729del

Select item 14696589598.

rs1469658959 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:113744627 (GRCh38)
12:114182432 (GRCh37)
Canonical SPDI:: NC_000012.12:113744626:C:T
Gene:: LINC01234 (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.113744627C>T, NC_000012.11:g.114182432C>T, NR_110026.1:n.2172G>A, NR_110025.1:n.2038G>A

Select item 14684781669.

rs1468478166 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 12:113746064 (GRCh38)
12:114183869 (GRCh37)
Canonical SPDI:: NC_000012.12:113746063:G:C
Gene:: LINC01234 (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.113746064G>C, NC_000012.11:g.114183869G>C, NR_110026.1:n.735C>G, NR_110025.1:n.601C>G

Select item 146790679810.

rs1467906798 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:113746142 (GRCh38)
12:114183947 (GRCh37)
Canonical SPDI:: NC_000012.12:113746141:G:A
Gene:: LINC01234 (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.113746142G>A, NC_000012.11:g.114183947G>A, NR_110026.1:n.657C>T, NR_110025.1:n.523C>T

Select item 146626151511.

rs1466261515 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:113745361 (GRCh38)
12:114183166 (GRCh37)
Canonical SPDI:: NC_000012.12:113745360:C:T
Gene:: LINC01234 (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.113745361C>T, NC_000012.11:g.114183166C>T, NR_110026.1:n.1438G>A, NR_110025.1:n.1304G>A

Select item 146196726312.

rs1461967263 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:113745539 (GRCh38)
12:114183344 (GRCh37)
Canonical SPDI:: NC_000012.12:113745538:C:A
Gene:: LINC01234 (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.113745539C>A, NC_000012.11:g.114183344C>A, NR_110026.1:n.1260G>T, NR_110025.1:n.1126G>T

Select item 145973543513.

rs1459735435 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:113746091 (GRCh38)
12:114183896 (GRCh37)
Canonical SPDI:: NC_000012.12:113746090:T:C
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.113746091T>C, NC_000012.11:g.114183896T>C, NR_110026.1:n.708A>G, NR_110025.1:n.574A>G

Select item 145955592514.

rs1459555925 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:113744870 (GRCh38)
12:114182675 (GRCh37)
Canonical SPDI:: NC_000012.12:113744869:G:A
Gene:: LINC01234 (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.113744870G>A, NC_000012.11:g.114182675G>A, NR_110026.1:n.1929C>T, NR_110025.1:n.1795C>T

Select item 145895001415.

rs1458950014 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:113746491 (GRCh38)
12:114184296 (GRCh37)
Canonical SPDI:: NC_000012.12:113746490:T:C
Gene:: LINC01234 (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.113746491T>C, NC_000012.11:g.114184296T>C, NR_110026.1:n.308A>G, NR_110025.1:n.174A>G

Select item 145748904416.

rs1457489044 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:113746587 (GRCh38)
12:114184392 (GRCh37)
Canonical SPDI:: NC_000012.12:113746586:G:A
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.113746587G>A, NC_000012.11:g.114184392G>A, NR_110026.1:n.212C>T, NR_110025.1:n.78C>T

Select item 145635150217.

rs1456351502 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGG>- [Show Flanks]
Chromosome:: 12:113767095 (GRCh38)
12:114204900 (GRCh37)
Canonical SPDI:: NC_000012.12:113767091:TGGTGG:TGG
Gene:: LINC01234 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TGGTGG=0./0 (ALFA)
-=0.000023/6 (TOPMED)
HGVS:: NC_000012.12:g.113767092TGG[1], NC_000012.11:g.114204897TGG[1], NR_110026.1:n.181CCA[1]

Select item 145461839518.

rs1454618395 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:113745067 (GRCh38)
12:114182872 (GRCh37)
Canonical SPDI:: NC_000012.12:113745066:T:G
Gene:: LINC01234 (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.113745067T>G, NC_000012.11:g.114182872T>G, NR_110026.1:n.1732A>C, NR_110025.1:n.1598A>C

Select item 145204651319.

rs1452046513 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 12:113746231 (GRCh38)
12:114184036 (GRCh37)
Canonical SPDI:: NC_000012.12:113746230:G:T
Gene:: LINC01234 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000012.12:g.113746231G>T, NC_000012.11:g.114184036G>T, NR_110026.1:n.568C>A, NR_110025.1:n.434C>A

Select item 145124765520.

rs1451247655 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:113745515 (GRCh38)
12:114183320 (GRCh37)
Canonical SPDI:: NC_000012.12:113745514:A:G
Gene:: LINC01234 (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=0.000015/4 (TOPMED)
HGVS:: NC_000012.12:g.113745515A>G, NC_000012.11:g.114183320A>G, NR_110026.1:n.1284T>C, NR_110025.1:n.1150T>C

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