SNP Links for Nucleotide (Select 671744855) - SNP

Links from Nucleotide

Items: 1 to 20 of 128

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Select item 14858248621.

rs1485824862 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:84620825 (GRCh38)
1:85086508 (GRCh37)
Canonical SPDI:: NC_000001.11:84620824:G:C
Gene:: LINC01461 (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=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.84620825G>C, NC_000001.10:g.85086508G>C, NR_125761.1:n.207C>G

Select item 14837517232.

rs1483751723 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:84620757 (GRCh38)
1:85086440 (GRCh37)
Canonical SPDI:: NC_000001.11:84620756:C:T
Gene:: LINC01461 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.84620757C>T, NC_000001.10:g.85086440C>T, NR_125761.1:n.275G>A

Select item 14752483603.

rs1475248360 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:84620904 (GRCh38)
1:85086587 (GRCh37)
Canonical SPDI:: NC_000001.11:84620903:G:A,NC_000001.11:84620903:G:T
Gene:: LINC01461 (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_000001.11:g.84620904G>A, NC_000001.11:g.84620904G>T, NC_000001.10:g.85086587G>A, NC_000001.10:g.85086587G>T, NR_125761.1:n.128C>T, NR_125761.1:n.128C>A

Select item 14749519694.

rs1474951969 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:84597967 (GRCh38)
1:85063650 (GRCh37)
Canonical SPDI:: NC_000001.11:84597966:G:A
Gene:: LINC01461 (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_000001.11:g.84597967G>A, NC_000001.10:g.85063650G>A, NR_125761.1:n.557C>T

Select item 14727387975.

rs1472738797 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:84598006 (GRCh38)
1:85063689 (GRCh37)
Canonical SPDI:: NC_000001.11:84598005:G:A
Gene:: LINC01461 (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_000001.11:g.84598006G>A, NC_000001.10:g.85063689G>A, NR_125761.1:n.518C>T

Select item 14722847466.

rs1472284746 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:84620996 (GRCh38)
1:85086679 (GRCh37)
Canonical SPDI:: NC_000001.11:84620995:G:A
Gene:: LINC01461 (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_000001.11:g.84620996G>A, NC_000001.10:g.85086679G>A, NR_125761.1:n.36C>T

Select item 14718670137.

rs1471867013 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:84620819 (GRCh38)
1:85086502 (GRCh37)
Canonical SPDI:: NC_000001.11:84620818:C:T
Gene:: LINC01461 (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_000001.11:g.84620819C>T, NC_000001.10:g.85086502C>T, NR_125761.1:n.213G>A

Select item 14658506338.

rs1465850633 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:84620813 (GRCh38)
1:85086496 (GRCh37)
Canonical SPDI:: NC_000001.11:84620812:A:T
Gene:: LINC01461 (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_000001.11:g.84620813A>T, NC_000001.10:g.85086496A>T, NR_125761.1:n.219T>A

Select item 14633798639.

rs1463379863 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:84621008 (GRCh38)
1:85086691 (GRCh37)
Canonical SPDI:: NC_000001.11:84621007:C:A
Gene:: LINC01461 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000001.11:g.84621008C>A, NC_000001.10:g.85086691C>A, NR_125761.1:n.24G>T

Select item 145614712110.

rs1456147121 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:84620898 (GRCh38)
1:85086581 (GRCh37)
Canonical SPDI:: NC_000001.11:84620897:T:C,NC_000001.11:84620897:T:G
Gene:: LINC01461 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.84620898T>C, NC_000001.11:g.84620898T>G, NC_000001.10:g.85086581T>C, NC_000001.10:g.85086581T>G, NR_125761.1:n.134A>G, NR_125761.1:n.134A>C

Select item 145321153311.

rs1453211533 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:84621019 (GRCh38)
1:85086702 (GRCh37)
Canonical SPDI:: NC_000001.11:84621018:G:A
Gene:: LINC01461 (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_000001.11:g.84621019G>A, NC_000001.10:g.85086702G>A, NR_125761.1:n.13C>T

Select item 143974061112.

rs1439740611 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:84621021 (GRCh38)
1:85086704 (GRCh37)
Canonical SPDI:: NC_000001.11:84621020:G:A,NC_000001.11:84621020:G:C
Gene:: LINC01461 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.84621021G>A, NC_000001.11:g.84621021G>C, NC_000001.10:g.85086704G>A, NC_000001.10:g.85086704G>C, NR_125761.1:n.11C>T, NR_125761.1:n.11C>G

Select item 143827485113.

rs1438274851 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:84618788 (GRCh38)
1:85084471 (GRCh37)
Canonical SPDI:: NC_000001.11:84618787:C:T
Gene:: LINC01461 (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_000001.11:g.84618788C>T, NC_000001.10:g.85084471C>T, NR_125761.1:n.372G>A

Select item 143560550414.

rs1435605504 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:84620799 (GRCh38)
1:85086482 (GRCh37)
Canonical SPDI:: NC_000001.11:84620798:T:G
Gene:: LINC01461 (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_000001.11:g.84620799T>G, NC_000001.10:g.85086482T>G, NR_125761.1:n.233A>C

Select item 142596491115.

rs1425964911 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 1:84597974 (GRCh38)
1:85063657 (GRCh37)
Canonical SPDI:: NC_000001.11:84597973:A:G,NC_000001.11:84597973:A:T
Gene:: LINC01461 (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)
HGVS:: NC_000001.11:g.84597974A>G, NC_000001.11:g.84597974A>T, NC_000001.10:g.85063657A>G, NC_000001.10:g.85063657A>T, NR_125761.1:n.550T>C, NR_125761.1:n.550T>A

Select item 142570478116.

rs1425704781 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:84597981 (GRCh38)
1:85063664 (GRCh37)
Canonical SPDI:: NC_000001.11:84597980:T:C
Gene:: LINC01461 (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_000001.11:g.84597981T>C, NC_000001.10:g.85063664T>C, NR_125761.1:n.543A>G

Select item 141536116617.

rs1415361166 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:84620988 (GRCh38)
1:85086671 (GRCh37)
Canonical SPDI:: NC_000001.11:84620987:G:C,NC_000001.11:84620987:G:T
Gene:: LINC01461 (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_000001.11:g.84620988G>C, NC_000001.11:g.84620988G>T, NC_000001.10:g.85086671G>C, NC_000001.10:g.85086671G>T, NR_125761.1:n.44C>G, NR_125761.1:n.44C>A

Select item 141400970218.

rs1414009702 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:84618762 (GRCh38)
1:85084445 (GRCh37)
Canonical SPDI:: NC_000001.11:84618761:C:T
Gene:: LINC01461 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.84618762C>T, NC_000001.10:g.85084445C>T, NR_125761.1:n.398G>A

Select item 138616008719.

rs1386160087 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:84620875 (GRCh38)
1:85086558 (GRCh37)
Canonical SPDI:: NC_000001.11:84620874:C:T
Gene:: LINC01461 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.84620875C>T, NC_000001.10:g.85086558C>T, NR_125761.1:n.157G>A

Select item 137946051820.

rs1379460518 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:84618808 (GRCh38)
1:85084491 (GRCh37)
Canonical SPDI:: NC_000001.11:84618807:G:A
Gene:: LINC01461 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.84618808G>A, NC_000001.10:g.85084491G>A, NR_125761.1:n.352C>T

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Links from Nucleotide

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