SNP Links for Nucleotide (Select 224967097) - SNP

Links from Nucleotide

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Select item 14899117511.

rs1489911751 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:123018398 (GRCh38)
11:122889106 (GRCh37)
Canonical SPDI:: NC_000011.10:123018397:G:C
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.123018398G>C, NC_000011.9:g.122889106G>C, NR_027288.1:n.833G>C

Select item 14894809112.

rs1489480911 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTC>- [Show Flanks]
Chromosome:: 11:123018614 (GRCh38)
11:122889322 (GRCh37)
Canonical SPDI:: NC_000011.10:123018606:CTTCTTCTTC:CTTCTTC
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTTCTTC=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.123018608TTC[2], NC_000011.9:g.122889316TTC[2], NR_027288.1:n.1043TTC[2]

Select item 14864330913.

rs1486433091 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:123019401 (GRCh38)
11:122890109 (GRCh37)
Canonical SPDI:: NC_000011.10:123019400:C:T
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.123019401C>T, NC_000011.9:g.122890109C>T, NR_027288.1:n.1836C>T

Select item 14859971224.

rs1485997122 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:123018964 (GRCh38)
11:122889672 (GRCh37)
Canonical SPDI:: NC_000011.10:123018963:T:C
Gene:: LOC341056 (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=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.123018964T>C, NC_000011.9:g.122889672T>C, NR_027288.1:n.1399T>C

Select item 14853084855.

rs1485308485 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:123018138 (GRCh38)
11:122888846 (GRCh37)
Canonical SPDI:: NC_000011.10:123018137:C:T
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.123018138C>T, NC_000011.9:g.122888846C>T, NR_027288.1:n.573C>T

Select item 14835217456.

rs1483521745 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:123018079 (GRCh38)
11:122888787 (GRCh37)
Canonical SPDI:: NC_000011.10:123018078:C:A
Gene:: LOC341056 (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_000011.10:g.123018079C>A, NC_000011.9:g.122888787C>A, NR_027288.1:n.514C>A

Select item 14830543667.

rs1483054366 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:123019382 (GRCh38)
11:122890090 (GRCh37)
Canonical SPDI:: NC_000011.10:123019381:T:A
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.123019382T>A, NC_000011.9:g.122890090T>A, NR_027288.1:n.1817T>A

Select item 14794684818.

rs1479468481 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 11:123018117 (GRCh38)
11:122888825 (GRCh37)
Canonical SPDI:: NC_000011.10:123018116:G:C,NC_000011.10:123018116:G:T
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000007/1 (GnomAD)
G=0.5/2 (SGDP_PRJ)
HGVS:: NC_000011.10:g.123018117G>C, NC_000011.10:g.123018117G>T, NC_000011.9:g.122888825G>C, NC_000011.9:g.122888825G>T, NR_027288.1:n.552G>C, NR_027288.1:n.552G>T

Select item 14790798969.

rs1479079896 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:123017870 (GRCh38)
11:122888578 (GRCh37)
Canonical SPDI:: NC_000011.10:123017869:A:G
Gene:: LOC341056 (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_000011.10:g.123017870A>G, NC_000011.9:g.122888578A>G, NR_027288.1:n.305A>G

Select item 147548148910.

rs1475481489 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:123019044 (GRCh38)
11:122889752 (GRCh37)
Canonical SPDI:: NC_000011.10:123019043:A:G
Gene:: LOC341056 (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_000011.10:g.123019044A>G, NC_000011.9:g.122889752A>G, NR_027288.1:n.1479A>G

Select item 147483463311.

rs1474834633 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:123018249 (GRCh38)
11:122888957 (GRCh37)
Canonical SPDI:: NC_000011.10:123018248:C:T
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.123018249C>T, NC_000011.9:g.122888957C>T, NR_027288.1:n.684C>T

Select item 147325831112.

rs1473258311 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:123017585 (GRCh38)
11:122888293 (GRCh37)
Canonical SPDI:: NC_000011.10:123017584:T:C,NC_000011.10:123017584:T:G
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000029/4 (GnomAD)
G=0.002747/8 (KOREAN)
HGVS:: NC_000011.10:g.123017585T>C, NC_000011.10:g.123017585T>G, NC_000011.9:g.122888293T>C, NC_000011.9:g.122888293T>G, NR_027288.1:n.20T>C, NR_027288.1:n.20T>G

Select item 147052418813.

rs1470524188 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:123019367 (GRCh38)
11:122890075 (GRCh37)
Canonical SPDI:: NC_000011.10:123019366:T:C
Gene:: LOC341056 (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=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.123019367T>C, NC_000011.9:g.122890075T>C, NR_027288.1:n.1802T>C

Select item 146983231714.

rs1469832317 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:123017639 (GRCh38)
11:122888347 (GRCh37)
Canonical SPDI:: NC_000011.10:123017638:A:G
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.123017639A>G, NC_000011.9:g.122888347A>G, NR_027288.1:n.74A>G

Select item 146728059015.

rs1467280590 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:123017945 (GRCh38)
11:122888653 (GRCh37)
Canonical SPDI:: NC_000011.10:123017944:T:C
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.123017945T>C, NC_000011.9:g.122888653T>C, NR_027288.1:n.380T>C

Select item 146700396716.

rs1467003967 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:123018042 (GRCh38)
11:122888750 (GRCh37)
Canonical SPDI:: NC_000011.10:123018041:C:A
Gene:: LOC341056 (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_000011.10:g.123018042C>A, NC_000011.9:g.122888750C>A, NR_027288.1:n.477C>A

Select item 146686499517.

rs1466864995 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:123017893 (GRCh38)
11:122888601 (GRCh37)
Canonical SPDI:: NC_000011.10:123017892:G:A
Gene:: LOC341056 (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_000011.10:g.123017893G>A, NC_000011.9:g.122888601G>A, NR_027288.1:n.328G>A

Select item 146396417618.

rs1463964176 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:123018814 (GRCh38)
11:122889522 (GRCh37)
Canonical SPDI:: NC_000011.10:123018813:G:A
Gene:: LOC341056 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (Korea1K)
A=0.000026/7 (TOPMED)
HGVS:: NC_000011.10:g.123018814G>A, NC_000011.9:g.122889522G>A, NR_027288.1:n.1249G>A

Select item 146050321519.

rs1460503215 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:123018331 (GRCh38)
11:122889039 (GRCh37)
Canonical SPDI:: NC_000011.10:123018330:T:C
Gene:: LOC341056 (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_000011.10:g.123018331T>C, NC_000011.9:g.122889039T>C, NR_027288.1:n.766T>C

Select item 146008305120.

rs1460083051 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:123017866 (GRCh38)
11:122888574 (GRCh37)
Canonical SPDI:: NC_000011.10:123017865:C:T
Gene:: LOC341056 (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_000011.10:g.123017866C>T, NC_000011.9:g.122888574C>T, NR_027288.1:n.301C>T

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