SNP Links for Nucleotide (Select 1194445967) - SNP

Links from Nucleotide

Items: 1 to 20 of 263

<< First< Prev

Page of 14

Next >Last >>

Select item 14848724661.

rs1484872466 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 12:126401162 (GRCh38)
12:126885708 (GRCh37)
Canonical SPDI:: NC_000012.12:126401161:A:C
Gene:: LINC02825 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000132/2 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000446/2 (Estonian)
HGVS:: NC_000012.12:g.126401162A>C, NC_000012.11:g.126885708A>C, NW_003315940.1:g.180007A>C, NR_147498.1:n.863T>G

Select item 14845651972.

rs1484565197 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 12:126401694 (GRCh38)
12:126886240 (GRCh37)
Canonical SPDI:: NC_000012.12:126401693:T:A,NC_000012.12:126401693:T:C
Gene:: LINC02825 (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)
C=0.000342/1 (KOREAN)
C=0.000389/7 (TOMMO)
HGVS:: NC_000012.12:g.126401694T>A, NC_000012.12:g.126401694T>C, NC_000012.11:g.126886240T>A, NC_000012.11:g.126886240T>C, NW_003315940.1:g.180539T>A, NW_003315940.1:g.180539T>C, NR_147498.1:n.331A>T, NR_147498.1:n.331A>G

Select item 14843769213.

rs1484376921 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:126401470 (GRCh38)
12:126886016 (GRCh37)
Canonical SPDI:: NC_000012.12:126401469:C:G
Gene:: LINC02825 (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.126401470C>G, NC_000012.11:g.126886016C>G, NW_003315940.1:g.180315C>G, NR_147498.1:n.555G>C

Select item 14718359804.

rs1471835980 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 12:126401478 (GRCh38)
12:126886024 (GRCh37)
Canonical SPDI:: NC_000012.12:126401477:T:A,NC_000012.12:126401477:T:G
Gene:: LINC02825 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000023/6 (TOPMED)
A=0.000425/7 (TOMMO)
A=0.001369/4 (KOREAN)
HGVS:: NC_000012.12:g.126401478T>A, NC_000012.12:g.126401478T>G, NC_000012.11:g.126886024T>A, NC_000012.11:g.126886024T>G, NW_003315940.1:g.180323T>A, NW_003315940.1:g.180323T>G, NR_147498.1:n.547A>T, NR_147498.1:n.547A>C

Select item 14696827615.

rs1469682761 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 12:126401513 (GRCh38)
12:126886059 (GRCh37)
Canonical SPDI:: NC_000012.12:126401512:C:A,NC_000012.12:126401512:C:T
Gene:: LINC02825 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.126401513C>A, NC_000012.12:g.126401513C>T, NC_000012.11:g.126886059C>A, NC_000012.11:g.126886059C>T, NW_003315940.1:g.180358C>A, NW_003315940.1:g.180358C>T, NR_147498.1:n.512G>T, NR_147498.1:n.512G>A

Select item 14696374596.

rs1469637459 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:126405497 (GRCh38)
12:126890043 (GRCh37)
Canonical SPDI:: NC_000012.12:126405496:C:T
Gene:: LINC02825 (Varview), LOC124903048 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000038/10 (TOPMED)
HGVS:: NC_000012.12:g.126405497C>T, NC_000012.11:g.126890043C>T, NR_147498.1:n.291G>A

Select item 14680989027.

rs1468098902 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:126400793 (GRCh38)
12:126885339 (GRCh37)
Canonical SPDI:: NC_000012.12:126400792:T:C
Gene:: LINC02825 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000012.12:g.126400793T>C, NC_000012.11:g.126885339T>C, NW_003315940.1:g.179638T>C, NR_147498.1:n.1232A>G

Select item 14678939358.

rs1467893935 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:126405472 (GRCh38)
12:126890018 (GRCh37)
Canonical SPDI:: NC_000012.12:126405471:T:C
Gene:: LINC02825 (Varview), LOC124903048 (Varview)
Functional Consequence:: intron_variant,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.126405472T>C, NC_000012.11:g.126890018T>C, NW_003315940.1:g.184317T>C, NR_147498.1:n.316A>G

Select item 14675958479.

rs1467595847 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:126445533 (GRCh38)
12:126930079 (GRCh37)
Canonical SPDI:: NC_000012.12:126445532:T:G
Gene:: LINC02825 (Varview), LINC02347 (Varview)
Functional Consequence:: intron_variant,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.126445533T>G, NC_000012.11:g.126930079T>G, NR_147498.1:n.146A>C

Select item 146757201210.

rs1467572012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 12:126401646 (GRCh38)
12:126886192 (GRCh37)
Canonical SPDI:: NC_000012.12:126401645:C:A,NC_000012.12:126401645:C:T
Gene:: LINC02825 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
A=0.000156/1 (1000Genomes)
HGVS:: NC_000012.12:g.126401646C>A, NC_000012.12:g.126401646C>T, NC_000012.11:g.126886192C>A, NC_000012.11:g.126886192C>T, NW_003315940.1:g.180491C>A, NW_003315940.1:g.180491C>T, NR_147498.1:n.379G>T, NR_147498.1:n.379G>A

Select item 146608665611.

rs1466086656 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:126401541 (GRCh38)
12:126886087 (GRCh37)
Canonical SPDI:: NC_000012.12:126401540:C:T
Gene:: LINC02825 (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.126401541C>T, NC_000012.11:g.126886087C>T, NW_003315940.1:g.180386C>T, NR_147498.1:n.484G>A

Select item 146498949912.

rs1464989499 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGCT>- [Show Flanks]
Chromosome:: 12:126445464 (GRCh38)
12:126930010 (GRCh37)
Canonical SPDI:: NC_000012.12:126445456:GCTGGCTGGCT:GCTGGCT
Gene:: LINC02825 (Varview), LINC02347 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GCTGGCT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.126445460GGCT[1], NC_000012.11:g.126930006GGCT[1], NR_147498.1:n.215CAGC[1]

Select item 146012477813.

rs1460124778 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:126405506 (GRCh38)
12:126890052 (GRCh37)
Canonical SPDI:: NC_000012.12:126405505:C:T
Gene:: LINC02825 (Varview), LOC124903048 (Varview)
Functional Consequence:: intron_variant,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.126405506C>T, NC_000012.11:g.126890052C>T, NR_147498.1:n.282G>A

Select item 145891677714.

rs1458916777 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:126401275 (GRCh38)
12:126885821 (GRCh37)
Canonical SPDI:: NC_000012.12:126401274:G:A
Gene:: LINC02825 (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.126401275G>A, NC_000012.11:g.126885821G>A, NW_003315940.1:g.180120G>A, NR_147498.1:n.750C>T

Select item 145680161515.

rs1456801615 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 12:126445433 (GRCh38)
12:126929979 (GRCh37)
Canonical SPDI:: NC_000012.12:126445432:GG:G
Gene:: LINC02825 (Varview), LINC02347 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.126445434del, NC_000012.11:g.126929980del, NR_147498.1:n.246del

Select item 145613074216.

rs1456130742 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 12:126401294 (GRCh38)
12:126885840 (GRCh37)
Canonical SPDI:: NC_000012.12:126401293:A:T
Gene:: LINC02825 (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.126401294A>T, NC_000012.11:g.126885840A>T, NW_003315940.1:g.180139A>T, NR_147498.1:n.731T>A

Select item 145426415617.

rs1454264156 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:126400894 (GRCh38)
12:126885440 (GRCh37)
Canonical SPDI:: NC_000012.12:126400893:T:C
Gene:: LINC02825 (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.126400894T>C, NC_000012.11:g.126885440T>C, NW_003315940.1:g.179739T>C, NR_147498.1:n.1131A>G

Select item 145256692618.

rs1452566926 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:126401403 (GRCh38)
12:126885949 (GRCh37)
Canonical SPDI:: NC_000012.12:126401402:C:A
Gene:: LINC02825 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.126401403C>A, NC_000012.11:g.126885949C>A, NW_003315940.1:g.180248C>A, NR_147498.1:n.622G>T

Select item 145035038419.

rs1450350384 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:126400916 (GRCh38)
12:126885462 (GRCh37)
Canonical SPDI:: NC_000012.12:126400915:C:A
Gene:: LINC02825 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.126400916C>A, NC_000012.11:g.126885462C>A, NW_003315940.1:g.179761C>A, NR_147498.1:n.1109G>T

Select item 144927563720.

rs1449275637 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:126449303 (GRCh38)
12:126933849 (GRCh37)
Canonical SPDI:: NC_000012.12:126449302:C:T
Gene:: LINC02825 (Varview), LINC02347 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.126449303C>T, NC_000012.11:g.126933849C>T, NR_147498.1:n.25G>A

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 263

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity