SNP Links for Nucleotide (Select 225703125) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Nucleotide

Items: 1 to 20 of 891

<< First< Prev

Page of 45

Next >Last >>

Select item 14906208231.

rs1490620823 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 15:23163958 (GRCh38)
15:22709110 (GRCh37)
Canonical SPDI:: NC_000015.10:23163957:T:C,NC_000015.10:23163957:T:G
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.23163958T>C, NC_000015.10:g.23163958T>G, NC_000015.9:g.22709110A>G, NC_000015.9:g.22709110A>C, NW_021160017.1:g.4058720T>C, NW_021160017.1:g.4058720T>G, NT_187603.1:g.264466T>C, NT_187603.1:g.264466T>G, NT_187659.1:g.133468T>C, NT_187659.1:g.133468T>G, NR_027407.1:n.1404T>C, NR_027407.1:n.1404T>G

Select item 14901230282.

rs1490123028 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:23162883 (GRCh38)
15:22710185 (GRCh37)
Canonical SPDI:: NC_000015.10:23162882:G:C
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00011/2 (GnomAD)
HGVS:: NC_000015.10:g.23162883G>C, NC_000015.9:g.22710185C>G, NW_021160017.1:g.4057646G>C, NT_187603.1:g.263391G>C, NT_187659.1:g.132393G>C, NR_027407.1:n.1019G>C

Select item 14892491303.

rs1489249130 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 15:23167627 (GRCh38)
15:22705441 (GRCh37)
Canonical SPDI:: NC_000015.10:23167626:G:A,NC_000015.10:23167626:G:T
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.23167627G>A, NC_000015.10:g.23167627G>T, NC_000015.9:g.22705441C>T, NC_000015.9:g.22705441C>A, NW_021160017.1:g.4062389G>A, NW_021160017.1:g.4062389G>T, NT_187603.1:g.268135G>A, NT_187603.1:g.268135G>T, NT_187659.1:g.137137G>A, NT_187659.1:g.137137G>T, NR_027407.1:n.2183G>A, NR_027407.1:n.2183G>T

Select item 14890402414.

rs1489040241 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:23167689 (GRCh38)
15:22705379 (GRCh37)
Canonical SPDI:: NC_000015.10:23167688:C:T
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000015.10:g.23167689C>T, NC_000015.9:g.22705379G>A, NW_021160017.1:g.4062451C>T, NT_187603.1:g.268197C>T, NT_187659.1:g.137199C>T, NR_027407.1:n.2245C>T

Select item 14889547935.

rs1488954793 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: 15:23168032 (GRCh38)
15:22705036 (GRCh37)
Canonical SPDI:: NC_000015.10:23168030:GTG:G
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000015.10:g.23168032_23168033del, NC_000015.9:g.22705036_22705037del, NW_021160017.1:g.4062794_4062795del, NT_187603.1:g.268540_268541del, NT_187659.1:g.137542_137543del, NR_027407.1:n.2588_2589del

Select item 14889329156.

rs1488932915 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:23169581 (GRCh38)
15:22703487 (GRCh37)
Canonical SPDI:: NC_000015.10:23169580:C:T
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/1 (GnomAD)
T=0.000319/5 (TOMMO)
HGVS:: NC_000015.10:g.23169581C>T, NC_000015.9:g.22703487G>A, NW_021160017.1:g.4064343C>T, NT_187603.1:g.270089C>T, NT_187659.1:g.139091C>T, NR_027407.1:n.4137C>T

Select item 14881711127.

rs1488171112 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:23166386 (GRCh38)
15:22706682 (GRCh37)
Canonical SPDI:: NC_000015.10:23166385:A:G
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000843/10 (ALFA)
C=0.000516/29 (GnomAD_exomes)
G=0.000739/102 (GnomAD)
G=0.002342/15 (1000Genomes)
T=0.5/1 (SGDP_PRJ)
HGVS:: NC_000015.10:g.23166386A>G, NC_000015.9:g.22706682T>C, NW_021160017.1:g.4061148A>G, NT_187603.1:g.266894A>G, NT_187659.1:g.135896A>G, NR_027407.1:n.1766A>G

Select item 14880598908.

rs1488059890 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:23163145 (GRCh38)
15:22709923 (GRCh37)
Canonical SPDI:: NC_000015.10:23163144:A:G
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000015.10:g.23163145A>G, NC_000015.9:g.22709923T>C, NW_021160017.1:g.4057908A>G, NT_187603.1:g.263653A>G, NT_187659.1:g.132655A>G, NR_027407.1:n.1175A>G

Select item 14871864879.

rs1487186487 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:23164392 (GRCh38)
15:22708676 (GRCh37)
Canonical SPDI:: NC_000015.10:23164391:G:A
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00003/2 (GnomAD)
T=0.00005/1 (GnomAD_exomes)
A=0.00016/1 (1000Genomes)
HGVS:: NC_000015.10:g.23164392G>A, NC_000015.9:g.22708676C>T, NW_021160017.1:g.4059154G>A, NT_187603.1:g.264900G>A, NT_187659.1:g.133902G>A, NR_027407.1:n.1571G>A

Select item 148700193910.

rs1487001939 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:23167761 (GRCh38)
15:22705307 (GRCh37)
Canonical SPDI:: NC_000015.10:23167760:A:G
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.23167761A>G, NC_000015.9:g.22705307T>C, NW_021160017.1:g.4062523A>G, NT_187603.1:g.268269A>G, NT_187659.1:g.137271A>G, NR_027407.1:n.2317A>G

Select item 148696413011.

rs1486964130 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 15:23167796 (GRCh38)
15:22705272 (GRCh37)
Canonical SPDI:: NC_000015.10:23167795:G:C,NC_000015.10:23167795:G:T
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.23167796G>C, NC_000015.10:g.23167796G>T, NC_000015.9:g.22705272C>G, NC_000015.9:g.22705272C>A, NW_021160017.1:g.4062558G>C, NW_021160017.1:g.4062558G>T, NT_187603.1:g.268304G>C, NT_187603.1:g.268304G>T, NT_187659.1:g.137306G>C, NT_187659.1:g.137306G>T, NR_027407.1:n.2352G>C, NR_027407.1:n.2352G>T

Select item 148686758012.

rs1486867580 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:23167193 (GRCh38)
15:22705875 (GRCh37)
Canonical SPDI:: NC_000015.10:23167192:C:T
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00008/1 (ALFA)
A=0.00077/7 (TOMMO)
HGVS:: NC_000015.10:g.23167193C>T, NC_000015.9:g.22705875G>A, NW_021160017.1:g.4061955C>T, NT_187603.1:g.267701C>T, NT_187659.1:g.136703C>T, NR_027407.1:n.1923C>T

Select item 148651385113.

rs1486513851 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:23159971 (GRCh38)
15:22713097 (GRCh37)
Canonical SPDI:: NC_000015.10:23159970:T:C
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.23159971T>C, NC_000015.9:g.22713097A>G, NW_021160017.1:g.4054734T>C, NT_187603.1:g.260479T>C, NT_187659.1:g.129481T>C, NR_027407.1:n.348T>C

Select item 148585205814.

rs1485852058 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:23163072 (GRCh38)
15:22709996 (GRCh37)
Canonical SPDI:: NC_000015.10:23163071:C:A
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000015.10:g.23163072C>A, NC_000015.9:g.22709996G>T, NW_021160017.1:g.4057835C>A, NT_187603.1:g.263580C>A, NT_187659.1:g.132582C>A, NR_027407.1:n.1102C>A

Select item 148572589115.

rs1485725891 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:23169752 (GRCh38)
15:22703316 (GRCh37)
Canonical SPDI:: NC_000015.10:23169751:T:C
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.23169752T>C, NC_000015.9:g.22703316A>G, NW_021160017.1:g.4064514T>C, NT_187603.1:g.270260T>C, NT_187659.1:g.139262T>C, NR_027407.1:n.4308T>C

Select item 148522844516.

rs1485228445 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:23170613 (GRCh38)
15:22702455 (GRCh37)
Canonical SPDI:: NC_000015.10:23170612:A:C
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00556/66 (ALFA)
C=0.00501/128 (GnomAD)
HGVS:: NC_000015.10:g.23170613A>C, NC_000015.9:g.22702455T>G, NW_021160017.1:g.4065375A>C, NT_187603.1:g.271121A>C, NT_187659.1:g.140123A>C, NR_027407.1:n.5169A>C

Select item 148488754617.

rs1484887546 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 15:23167960 (GRCh38)
15:22705105 (GRCh37)
Canonical SPDI:: NC_000015.10:23167960:TTT:TTTT
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
T=0.000028/3 (GnomAD)
HGVS:: NC_000015.10:g.23167963dup, NC_000015.9:g.22705107dup, NW_021160017.1:g.4062725dup, NT_187603.1:g.268471dup, NT_187659.1:g.137473dup, NR_027407.1:n.2519dup

Select item 148401779418.

rs1484017794 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:23169608 (GRCh38)
15:22703460 (GRCh37)
Canonical SPDI:: NC_000015.10:23169607:C:G,NC_000015.10:23169607:C:T
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000016/2 (GnomAD)
T=0.000156/1 (1000Genomes)
HGVS:: NC_000015.10:g.23169608C>G, NC_000015.10:g.23169608C>T, NC_000015.9:g.22703460G>C, NC_000015.9:g.22703460G>A, NW_021160017.1:g.4064370C>G, NW_021160017.1:g.4064370C>T, NT_187603.1:g.270116C>G, NT_187603.1:g.270116C>T, NT_187659.1:g.139118C>G, NT_187659.1:g.139118C>T, NR_027407.1:n.4164C>G, NR_027407.1:n.4164C>T

Select item 148393887419.

rs1483938874 has merged into rs755029146 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAG>- [Show Flanks]
Chromosome:: 15:23163368 (GRCh38)
15:22709702 (GRCh37)
Canonical SPDI:: NC_000015.10:23163363:GAAGAAG:GAAG
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAAG=0.000071/1 (ALFA)
-=0.000017/4 (GnomAD_exomes)
-=0.000027/3 (ExAC)
-=0.000312/2 (1000Genomes)
HGVS:: NC_000015.10:g.23163365AAG[1], NC_000015.9:g.22709699TTC[1], NW_021160017.1:g.4058127AAG[1], NT_187603.1:g.263873AAG[1], NT_187659.1:g.132875AAG[1], NR_027407.1:n.1199AAG[1]

Select item 148290705920.

rs1482907059 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:23167449 (GRCh38)
15:22705619 (GRCh37)
Canonical SPDI:: NC_000015.10:23167448:C:T
Gene:: GOLGA8DP (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00007/1 (GnomAD)
HGVS:: NC_000015.10:g.23167449C>T, NC_000015.9:g.22705619G>A, NW_021160017.1:g.4062211C>T, NT_187603.1:g.267957C>T, NT_187659.1:g.136959C>T, NR_027407.1:n.2090C>T

<< First< Prev

Page of 45

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Nucleotide (Select 225703125) (891)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: