SNP Links for Nucleotide (Select 560879487) - SNP

Links from Nucleotide

Items: 1 to 20 of 145

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Select item 14821918481.

rs1482191848 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 5:97504786 (GRCh38)
5:96840490 (GRCh37)
Canonical SPDI:: NC_000005.10:97504785:T:A,NC_000005.10:97504785:T:C
Gene:: LINC01340 (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_000005.10:g.97504786T>A, NC_000005.10:g.97504786T>C, NC_000005.9:g.96840490T>A, NC_000005.9:g.96840490T>C, NR_105028.1:n.91T>A, NR_105028.1:n.91T>C

Select item 14754973472.

rs1475497347 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:97521277 (GRCh38)
5:96856981 (GRCh37)
Canonical SPDI:: NC_000005.10:97521276:T:C
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.97521277T>C, NC_000005.9:g.96856981T>C, NR_105028.1:n.146T>C

Select item 14749844063.

rs1474984406 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:97671044 (GRCh38)
5:97006748 (GRCh37)
Canonical SPDI:: NC_000005.10:97671043:T:C
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000026/7 (TOPMED)
HGVS:: NC_000005.10:g.97671044T>C, NC_000005.9:g.97006748T>C, NR_105028.1:n.722T>C

Select item 14738586544.

rs1473858654 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:97668563 (GRCh38)
5:97004267 (GRCh37)
Canonical SPDI:: NC_000005.10:97668562:C:T
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.97668563C>T, NC_000005.9:g.97004267C>T, NR_105028.1:n.172C>T

Select item 14690135335.

rs1469013533 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 5:97670715 (GRCh38)
5:97006419 (GRCh37)
Canonical SPDI:: NC_000005.10:97670714:C:G
Gene:: LINC01340 (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_000005.10:g.97670715C>G, NC_000005.9:g.97006419C>G, NR_105028.1:n.393C>G

Select item 14665175206.

rs1466517520 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 5:97668659 (GRCh38)
5:97004363 (GRCh37)
Canonical SPDI:: NC_000005.10:97668658:T:G
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.97668659T>G, NC_000005.9:g.97004363T>G, NR_105028.1:n.268T>G

Select item 14523204707.

rs1452320470 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 5:97668578 (GRCh38)
5:97004282 (GRCh37)
Canonical SPDI:: NC_000005.10:97668577:A:T
Gene:: LINC01340 (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_000005.10:g.97668578A>T, NC_000005.9:g.97004282A>T, NR_105028.1:n.187A>T

Select item 14509823328.

rs1450982332 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:97521266 (GRCh38)
5:96856970 (GRCh37)
Canonical SPDI:: NC_000005.10:97521265:G:C
Gene:: LINC01340 (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_000005.10:g.97521266G>C, NC_000005.9:g.96856970G>C, NR_105028.1:n.135G>C

Select item 14506368429.

rs1450636842 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:97670821 (GRCh38)
5:97006525 (GRCh37)
Canonical SPDI:: NC_000005.10:97670820:G:T
Gene:: LINC01340 (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_000005.10:g.97670821G>T, NC_000005.9:g.97006525G>T, NR_105028.1:n.499G>T

Select item 144620069310.

rs1446200693 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 5:97670934 (GRCh38)
5:97006638 (GRCh37)
Canonical SPDI:: NC_000005.10:97670933:C:A,NC_000005.10:97670933:C:T
Gene:: LINC01340 (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)
HGVS:: NC_000005.10:g.97670934C>A, NC_000005.10:g.97670934C>T, NC_000005.9:g.97006638C>A, NC_000005.9:g.97006638C>T, NR_105028.1:n.612C>A, NR_105028.1:n.612C>T

Select item 143553693211.

rs1435536932 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:97670639 (GRCh38)
5:97006343 (GRCh37)
Canonical SPDI:: NC_000005.10:97670638:C:T
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000005.10:g.97670639C>T, NC_000005.9:g.97006343C>T, NR_105028.1:n.317C>T

Select item 143192575112.

rs1431925751 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:97670610 (GRCh38)
5:97006314 (GRCh37)
Canonical SPDI:: NC_000005.10:97670609:A:G
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.97670610A>G, NC_000005.9:g.97006314A>G, NR_105028.1:n.288A>G

Select item 142913970713.

rs1429139707 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:97670973 (GRCh38)
5:97006677 (GRCh37)
Canonical SPDI:: NC_000005.10:97670972:G:A
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000005.10:g.97670973G>A, NC_000005.9:g.97006677G>A, NR_105028.1:n.651G>A

Select item 142015712514.

rs1420157125 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:97504778 (GRCh38)
5:96840482 (GRCh37)
Canonical SPDI:: NC_000005.10:97504777:T:C
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.97504778T>C, NC_000005.9:g.96840482T>C, NR_105028.1:n.83T>C

Select item 140378872715.

rs1403788727 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:97670936 (GRCh38)
5:97006640 (GRCh37)
Canonical SPDI:: NC_000005.10:97670935:C:T
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000108/2 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000023/6 (TOPMED)
T=0.000223/1 (Estonian)
HGVS:: NC_000005.10:g.97670936C>T, NC_000005.9:g.97006640C>T, NR_105028.1:n.614C>T

Select item 139718346916.

rs1397183469 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 5:97671020 (GRCh38)
5:97006724 (GRCh37)
Canonical SPDI:: NC_000005.10:97671019:A:G,NC_000005.10:97671019:A:T
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.97671020A>G, NC_000005.10:g.97671020A>T, NC_000005.9:g.97006724A>G, NC_000005.9:g.97006724A>T, NR_105028.1:n.698A>G, NR_105028.1:n.698A>T

Select item 139625121217.

rs1396251212 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 5:97521254 (GRCh38)
5:96856958 (GRCh37)
Canonical SPDI:: NC_000005.10:97521253:A:C
Gene:: LINC01340 (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_000005.10:g.97521254A>C, NC_000005.9:g.96856958A>C, NR_105028.1:n.123A>C

Select item 139570497018.

rs1395704970 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 5:97670849 (GRCh38)
5:97006553 (GRCh37)
Canonical SPDI:: NC_000005.10:97670848:A:G,NC_000005.10:97670848:A:T
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000005.10:g.97670849A>G, NC_000005.10:g.97670849A>T, NC_000005.9:g.97006553A>G, NC_000005.9:g.97006553A>T, NR_105028.1:n.527A>G, NR_105028.1:n.527A>T

Select item 139277838219.

rs1392778382 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:97670661 (GRCh38)
5:97006365 (GRCh37)
Canonical SPDI:: NC_000005.10:97670660:T:C
Gene:: LINC01340 (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_000005.10:g.97670661T>C, NC_000005.9:g.97006365T>C, NR_105028.1:n.339T>C

Select item 138805788520.

rs1388057885 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 5:97670679 (GRCh38)
5:97006383 (GRCh37)
Canonical SPDI:: NC_000005.10:97670678:T:A,NC_000005.10:97670678:T:C
Gene:: LINC01340 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000005.10:g.97670679T>A, NC_000005.10:g.97670679T>C, NC_000005.9:g.97006383T>A, NC_000005.9:g.97006383T>C, NR_105028.1:n.357T>A, NR_105028.1:n.357T>C

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Links from Nucleotide

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