SNP Links for Nucleotide (Select 908212462) - SNP

Links from Nucleotide

Items: 1 to 20 of 559

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Select item 14871117711.

rs1487111771 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:96107408 (GRCh38)
9:98869690 (GRCh37)
Canonical SPDI:: NC_000009.12:96107407:A:C
Gene:: LOC158434 (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=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.96107408A>C, NC_000009.11:g.98869690A>C, NR_132344.1:n.1915T>G, NM_001256408.1:c.*1339T>G

Select item 14867933962.

rs1486793396 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:96108612 (GRCh38)
9:98870894 (GRCh37)
Canonical SPDI:: NC_000009.12:96108611:A:C
Gene:: LOC158434 (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_000009.12:g.96108612A>C, NC_000009.11:g.98870894A>C, NR_132344.1:n.711T>G, NM_001256408.1:c.*135T>G

Select item 14865755173.

rs1486575517 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:96108706 (GRCh38)
9:98870988 (GRCh37)
Canonical SPDI:: NC_000009.12:96108705:G:C
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.96108706G>C, NC_000009.11:g.98870988G>C, NR_132344.1:n.617C>G, NM_001256408.1:c.*41C>G

Select item 14860342334.

rs1486034233 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:96107283 (GRCh38)
9:98869565 (GRCh37)
Canonical SPDI:: NC_000009.12:96107282:T:C
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0./0 (KOREAN)
C=0.000015/4 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000009.12:g.96107283T>C, NC_000009.11:g.98869565T>C, NR_132344.1:n.2040A>G, NM_001256408.1:c.*1464A>G

Select item 14857958385.

rs1485795838 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:96108825 (GRCh38)
9:98871107 (GRCh37)
Canonical SPDI:: NC_000009.12:96108824:T:C
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.96108825T>C, NC_000009.11:g.98871107T>C, NR_132344.1:n.498A>G, NM_001256408.1:c.246A>G

Select item 14853780056.

rs1485378005 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:96108257 (GRCh38)
9:98870539 (GRCh37)
Canonical SPDI:: NC_000009.12:96108256:G:A
Gene:: LOC158434 (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_000009.12:g.96108257G>A, NC_000009.11:g.98870539G>A, NR_132344.1:n.1066C>T, NM_001256408.1:c.*490C>T

Select item 14851428247.

rs1485142824 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:96107423 (GRCh38)
9:98869705 (GRCh37)
Canonical SPDI:: NC_000009.12:96107422:G:C
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000009.12:g.96107423G>C, NC_000009.11:g.98869705G>C, NR_132344.1:n.1900C>G, NM_001256408.1:c.*1324C>G

Select item 14848745948.

rs1484874594 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:96114680 (GRCh38)
9:98876962 (GRCh37)
Canonical SPDI:: NC_000009.12:96114679:T:A
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000009.12:g.96114680T>A, NC_000009.11:g.98876962T>A, NR_132344.1:n.241A>T, NM_001256408.1:c.-12A>T

Select item 14838257429.

rs1483825742 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:96108432 (GRCh38)
9:98870714 (GRCh37)
Canonical SPDI:: NC_000009.12:96108431:T:C
Gene:: LOC158434 (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_000009.12:g.96108432T>C, NC_000009.11:g.98870714T>C, NR_132344.1:n.891A>G, NM_001256408.1:c.*315A>G

Select item 148070339810.

rs1480703398 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:96107652 (GRCh38)
9:98869934 (GRCh37)
Canonical SPDI:: NC_000009.12:96107651:T:C
Gene:: LOC158434 (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_000009.12:g.96107652T>C, NC_000009.11:g.98869934T>C, NR_132344.1:n.1671A>G, NM_001256408.1:c.*1095A>G

Select item 147978783711.

rs1479787837 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:96107065 (GRCh38)
9:98869347 (GRCh37)
Canonical SPDI:: NC_000009.12:96107064:G:A
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.96107065G>A, NC_000009.11:g.98869347G>A, NR_132344.1:n.2258C>T, NM_001256408.1:c.*1682C>T

Select item 147766713212.

rs1477667132 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:96106887 (GRCh38)
9:98869169 (GRCh37)
Canonical SPDI:: NC_000009.12:96106886:T:C
Gene:: LOC158434 (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_000009.12:g.96106887T>C, NC_000009.11:g.98869169T>C, NR_132344.1:n.2436A>G, NM_001256408.1:c.*1860A>G

Select item 147598582513.

rs1475985825 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:96106709 (GRCh38)
9:98868991 (GRCh37)
Canonical SPDI:: NC_000009.12:96106708:A:T
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000022/3 (GnomAD)
T=0.00003/8 (TOPMED)
HGVS:: NC_000009.12:g.96106709A>T, NC_000009.11:g.98868991A>T, NR_132344.1:n.2614T>A, NM_001256408.1:c.*2038T>A

Select item 147560106814.

rs1475601068 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:96107388 (GRCh38)
9:98869670 (GRCh37)
Canonical SPDI:: NC_000009.12:96107387:G:T
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.001027/3 (KOREAN)
HGVS:: NC_000009.12:g.96107388G>T, NC_000009.11:g.98869670G>T, NR_132344.1:n.1935C>A, NM_001256408.1:c.*1359C>A

Select item 147508220415.

rs1475082204 [Homo sapiens]

Variant type:: DELINS
Alleles:: CAA>- [Show Flanks]
Chromosome:: 9:96116370 (GRCh38)
9:98878652 (GRCh37)
Canonical SPDI:: NC_000009.12:96116365:ACAACAA:ACAA
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACAA=0.000432/8 (ALFA)
-=0.000121/32 (TOPMED)
-=0.000806/113 (GnomAD)
-=0.001786/8 (Estonian)
HGVS:: NC_000009.12:g.96116367CAA[1], NC_000009.11:g.98878649CAA[1], NR_132344.1:n.41TGT[1], NM_001256408.1:c.-212TGT[1]

Select item 147501211916.

rs1475012119 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:96107366 (GRCh38)
9:98869648 (GRCh37)
Canonical SPDI:: NC_000009.12:96107365:T:C
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000009.12:g.96107366T>C, NC_000009.11:g.98869648T>C, NR_132344.1:n.1957A>G, NM_001256408.1:c.*1381A>G

Select item 147439320217.

rs1474393202 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:96107999 (GRCh38)
9:98870281 (GRCh37)
Canonical SPDI:: NC_000009.12:96107998:C:T
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.96107999C>T, NC_000009.11:g.98870281C>T, NR_132344.1:n.1324G>A, NM_001256408.1:c.*748G>A

Select item 147429918918.

rs1474299189 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:96114646 (GRCh38)
9:98876928 (GRCh37)
Canonical SPDI:: NC_000009.12:96114645:C:A
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000016/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.96114646C>A, NC_000009.11:g.98876928C>A, NR_132344.1:n.275G>T, NM_001256408.1:c.23G>T

Select item 146718422719.

rs1467184227 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:96106662 (GRCh38)
9:98868944 (GRCh37)
Canonical SPDI:: NC_000009.12:96106661:A:T
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.00032/9 (TOMMO)
HGVS:: NC_000009.12:g.96106662A>T, NC_000009.11:g.98868944A>T, NR_132344.1:n.2661T>A, NM_001256408.1:c.*2085T>A

Select item 146661969520.

rs1466619695 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:96108418 (GRCh38)
9:98870700 (GRCh37)
Canonical SPDI:: NC_000009.12:96108417:T:A
Gene:: LOC158434 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.96108418T>A, NC_000009.11:g.98870700T>A, NR_132344.1:n.905A>T, NM_001256408.1:c.*329A>T

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