SNP Links for Nucleotide (Select 966001172) - SNP

Links from Nucleotide

Items: 1 to 20 of 172

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Select item 14901960561.

rs1490196056 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:132759131 (GRCh38)
7:132443891 (GRCh37)
Canonical SPDI:: NC_000007.14:132759130:A:G
Gene:: LOC100506937 (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_000007.14:g.132759131A>G, NC_000007.13:g.132443891A>G, NR_134332.1:n.162A>G

Select item 14898187782.

rs1489818778 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:132760563 (GRCh38)
7:132445323 (GRCh37)
Canonical SPDI:: NC_000007.14:132760562:C:G,NC_000007.14:132760562:C:T
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000008/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.132760563C>G, NC_000007.14:g.132760563C>T, NC_000007.13:g.132445323C>G, NC_000007.13:g.132445323C>T, NR_134332.1:n.682C>G, NR_134332.1:n.682C>T

Select item 14850106423.

rs1485010642 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:132759238 (GRCh38)
7:132443998 (GRCh37)
Canonical SPDI:: NC_000007.14:132759237:G:A,NC_000007.14:132759237:G:C
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.132759238G>A, NC_000007.14:g.132759238G>C, NC_000007.13:g.132443998G>A, NC_000007.13:g.132443998G>C, NR_134332.1:n.269G>A, NR_134332.1:n.269G>C

Select item 14801591944.

rs1480159194 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:132759224 (GRCh38)
7:132443984 (GRCh37)
Canonical SPDI:: NC_000007.14:132759223:C:G
Gene:: LOC100506937 (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_000007.14:g.132759224C>G, NC_000007.13:g.132443984C>G, NR_134332.1:n.255C>G

Select item 14789600915.

rs1478960091 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:132759117 (GRCh38)
7:132443877 (GRCh37)
Canonical SPDI:: NC_000007.14:132759116:G:C
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.132759117G>C, NC_000007.13:g.132443877G>C, NR_134332.1:n.148G>C

Select item 14660757576.

rs1466075757 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:132759304 (GRCh38)
7:132444064 (GRCh37)
Canonical SPDI:: NC_000007.14:132759303:G:A
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000007.14:g.132759304G>A, NC_000007.13:g.132444064G>A, NR_134332.1:n.335G>A

Select item 14630197727.

rs1463019772 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:132760345 (GRCh38)
7:132445105 (GRCh37)
Canonical SPDI:: NC_000007.14:132760344:T:C
Gene:: LOC100506937 (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_000007.14:g.132760345T>C, NC_000007.13:g.132445105T>C, NR_134332.1:n.464T>C

Select item 14545529028.

rs1454552902 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:132760370 (GRCh38)
7:132445130 (GRCh37)
Canonical SPDI:: NC_000007.14:132760369:G:C
Gene:: LOC100506937 (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_000007.14:g.132760370G>C, NC_000007.13:g.132445130G>C, NR_134332.1:n.489G>C

Select item 14499829659.

rs1449982965 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:132759284 (GRCh38)
7:132444044 (GRCh37)
Canonical SPDI:: NC_000007.14:132759283:C:G,NC_000007.14:132759283:C:T
Gene:: LOC100506937 (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_000007.14:g.132759284C>G, NC_000007.14:g.132759284C>T, NC_000007.13:g.132444044C>G, NC_000007.13:g.132444044C>T, NR_134332.1:n.315C>G, NR_134332.1:n.315C>T

Select item 144564555910.

rs1445645559 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:132759151 (GRCh38)
7:132443911 (GRCh37)
Canonical SPDI:: NC_000007.14:132759150:T:C
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.132759151T>C, NC_000007.13:g.132443911T>C, NR_134332.1:n.182T>C

Select item 144230565911.

rs1442305659 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:132759178 (GRCh38)
7:132443938 (GRCh37)
Canonical SPDI:: NC_000007.14:132759177:C:T
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000071/10 (GnomAD)
HGVS:: NC_000007.14:g.132759178C>T, NC_000007.13:g.132443938C>T, NR_134332.1:n.209C>T

Select item 142776184012.

rs1427761840 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:132760411 (GRCh38)
7:132445171 (GRCh37)
Canonical SPDI:: NC_000007.14:132760410:A:G
Gene:: LOC100506937 (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_000007.14:g.132760411A>G, NC_000007.13:g.132445171A>G, NR_134332.1:n.530A>G

Select item 142700562613.

rs1427005626 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:132759316 (GRCh38)
7:132444076 (GRCh37)
Canonical SPDI:: NC_000007.14:132759315:T:C
Gene:: LOC100506937 (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_000007.14:g.132759316T>C, NC_000007.13:g.132444076T>C, NR_134332.1:n.347T>C

Select item 142027104214.

rs1420271042 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 7:132760383 (GRCh38)
7:132445143 (GRCh37)
Canonical SPDI:: NC_000007.14:132760382:G:A,NC_000007.14:132760382:G:C,NC_000007.14:132760382:G:T
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000007.14:g.132760383G>A, NC_000007.14:g.132760383G>C, NC_000007.14:g.132760383G>T, NC_000007.13:g.132445143G>A, NC_000007.13:g.132445143G>C, NC_000007.13:g.132445143G>T, NR_134332.1:n.502G>A, NR_134332.1:n.502G>C, NR_134332.1:n.502G>T

Select item 141909934815.

rs1419099348 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:132759317 (GRCh38)
7:132444077 (GRCh37)
Canonical SPDI:: NC_000007.14:132759316:G:A
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.132759317G>A, NC_000007.13:g.132444077G>A, NR_134332.1:n.348G>A

Select item 141764258716.

rs1417642587 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:132759093 (GRCh38)
7:132443853 (GRCh37)
Canonical SPDI:: NC_000007.14:132759092:C:T
Gene:: LOC100506937 (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_000007.14:g.132759093C>T, NC_000007.13:g.132443853C>T, NR_134332.1:n.124C>T

Select item 140957689417.

rs1409576894 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:132760536 (GRCh38)
7:132445296 (GRCh37)
Canonical SPDI:: NC_000007.14:132760535:T:G
Gene:: LOC100506937 (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_000007.14:g.132760536T>G, NC_000007.13:g.132445296T>G, NR_134332.1:n.655T>G

Select item 140863613318.

rs1408636133 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:132759254 (GRCh38)
7:132444014 (GRCh37)
Canonical SPDI:: NC_000007.14:132759253:G:T
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.132759254G>T, NC_000007.13:g.132444014G>T, NR_134332.1:n.285G>T

Select item 140689070819.

rs1406890708 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:132759094 (GRCh38)
7:132443854 (GRCh37)
Canonical SPDI:: NC_000007.14:132759093:C:T
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000007.14:g.132759094C>T, NC_000007.13:g.132443854C>T, NR_134332.1:n.125C>T

Select item 140546711020.

rs1405467110 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGA>- [Show Flanks]
Chromosome:: 7:132758983 (GRCh38)
7:132443743 (GRCh37)
Canonical SPDI:: NC_000007.14:132758978:AAGAAGA:AAGA
Gene:: LOC100506937 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AAGA=0./0 (ALFA)
-=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.132758980AGA[1], NC_000007.13:g.132443740AGA[1], NR_134332.1:n.11AGA[1]

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