SNP Links for Nucleotide (Select 377823706) - SNP

Links from Nucleotide

Items: 1 to 20 of 127

<< First< Prev

Page of 7

Next >Last >>

Select item 14885014511.

rs1488501451 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:108728031 (GRCh38)
5:108063732 (GRCh37)
Canonical SPDI:: NC_000005.10:108728030:T:C
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.108728031T>C, NC_000005.9:g.108063732T>C, NR_046368.1:n.231A>G

Select item 14842241632.

rs1484224163 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 5:108727996 (GRCh38)
5:108063697 (GRCh37)
Canonical SPDI:: NC_000005.10:108727995:C:G
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.108727996C>G, NC_000005.9:g.108063697C>G, NR_046368.1:n.266G>C

Select item 14838449113.

rs1483844911 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 5:108728247 (GRCh38)
5:108063948 (GRCh37)
Canonical SPDI:: NC_000005.10:108728246:G:A,NC_000005.10:108728246:G:T
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.108728247G>A, NC_000005.10:g.108728247G>T, NC_000005.9:g.108063948G>A, NC_000005.9:g.108063948G>T, NR_046368.1:n.15C>T, NR_046368.1:n.15C>A

Select item 14819936344.

rs1481993634 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 5:108727921 (GRCh38)
5:108063622 (GRCh37)
Canonical SPDI:: NC_000005.10:108727920:C:A,NC_000005.10:108727920:C:T
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.108727921C>A, NC_000005.10:g.108727921C>T, NC_000005.9:g.108063622C>A, NC_000005.9:g.108063622C>T, NR_046368.1:n.341G>T, NR_046368.1:n.341G>A

Select item 14731166445.

rs1473116644 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:108728051 (GRCh38)
5:108063752 (GRCh37)
Canonical SPDI:: NC_000005.10:108728050:C:T
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.108728051C>T, NC_000005.9:g.108063752C>T, NR_046368.1:n.211G>A

Select item 14661177096.

rs1466117709 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 5:108728177 (GRCh38)
5:108063878 (GRCh37)
Canonical SPDI:: NC_000005.10:108728176:C:A,NC_000005.10:108728176:C:G,NC_000005.10:108728176:C:T
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000005.10:g.108728177C>A, NC_000005.10:g.108728177C>G, NC_000005.10:g.108728177C>T, NC_000005.9:g.108063878C>A, NC_000005.9:g.108063878C>G, NC_000005.9:g.108063878C>T, NR_046368.1:n.85G>T, NR_046368.1:n.85G>C, NR_046368.1:n.85G>A

Select item 14654429727.

rs1465442972 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>- [Show Flanks]
Chromosome:: 5:108728235 (GRCh38)
5:108063936 (GRCh37)
Canonical SPDI:: NC_000005.10:108728234:AAAAA:AAAA
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: AAAA=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.108728239del, NC_000005.9:g.108063940del, NR_046368.1:n.27del

Select item 14570077108.

rs1457007710 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 5:108727825 (GRCh38)
5:108063526 (GRCh37)
Canonical SPDI:: NC_000005.10:108727824:T:A
Gene:: LINC01023 (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_000005.10:g.108727825T>A, NC_000005.9:g.108063526T>A, NR_046368.1:n.437A>T

Select item 14565824509.

rs1456582450 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 5:108728210 (GRCh38)
5:108063911 (GRCh37)
Canonical SPDI:: NC_000005.10:108728209:C:G,NC_000005.10:108728209:C:T
Gene:: LINC01023 (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)
G=0.000106/2 (TOMMO)
G=0.00463/1 (Vietnamese)
HGVS:: NC_000005.10:g.108728210C>G, NC_000005.10:g.108728210C>T, NC_000005.9:g.108063911C>G, NC_000005.9:g.108063911C>T, NR_046368.1:n.52G>C, NR_046368.1:n.52G>A

Select item 145610337310.

rs1456103373 [Homo sapiens]

Variant type:: DELINS
Alleles:: GCA>- [Show Flanks]
Chromosome:: 5:108728067 (GRCh38)
5:108063768 (GRCh37)
Canonical SPDI:: NC_000005.10:108728062:AGCAGCA:AGCA
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGCA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
-=0.000223/1 (Estonian)
HGVS:: NC_000005.10:g.108728064GCA[1], NC_000005.9:g.108063765GCA[1], NR_046368.1:n.194GCT[1]

Select item 145090500311.

rs1450905003 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 5:108728151 (GRCh38)
5:108063852 (GRCh37)
Canonical SPDI:: NC_000005.10:108728150:A:C
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000084/1 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000005.10:g.108728151A>C, NC_000005.9:g.108063852A>C, NR_046368.1:n.111T>G

Select item 144110868112.

rs1441108681 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:108727885 (GRCh38)
5:108063586 (GRCh37)
Canonical SPDI:: NC_000005.10:108727884:T:C
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.00007/1 (ALFA)
HGVS:: NC_000005.10:g.108727885T>C, NC_000005.9:g.108063586T>C, NR_046368.1:n.377A>G

Select item 143874589313.

rs1438745893 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 5:108727914 (GRCh38)
5:108063615 (GRCh37)
Canonical SPDI:: NC_000005.10:108727913:C:A
Gene:: LINC01023 (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_000005.10:g.108727914C>A, NC_000005.9:g.108063615C>A, NR_046368.1:n.348G>T

Select item 143238832214.

rs1432388322 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:108728187 (GRCh38)
5:108063888 (GRCh37)
Canonical SPDI:: NC_000005.10:108728186:G:T
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.108728187G>T, NC_000005.9:g.108063888G>T, NR_046368.1:n.75C>A

Select item 142470249915.

rs1424702499 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 5:108727860 (GRCh38)
5:108063561 (GRCh37)
Canonical SPDI:: NC_000005.10:108727859:C:A
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.108727860C>A, NC_000005.9:g.108063561C>A, NR_046368.1:n.402G>T

Select item 141668200516.

rs1416682005 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 5:108728063 (GRCh38)
5:108063764 (GRCh37)
Canonical SPDI:: NC_000005.10:108728062:A:G,NC_000005.10:108728062:A:T
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000005.10:g.108728063A>G, NC_000005.10:g.108728063A>T, NC_000005.9:g.108063764A>G, NC_000005.9:g.108063764A>T, NR_046368.1:n.199T>C, NR_046368.1:n.199T>A

Select item 141660744017.

rs1416607440 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:108727908 (GRCh38)
5:108063609 (GRCh37)
Canonical SPDI:: NC_000005.10:108727907:G:C
Gene:: LINC01023 (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_000005.10:g.108727908G>C, NC_000005.9:g.108063609G>C, NR_046368.1:n.354C>G

Select item 140108492318.

rs1401084923 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:108728050 (GRCh38)
5:108063751 (GRCh37)
Canonical SPDI:: NC_000005.10:108728049:G:A
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.108728050G>A, NC_000005.9:g.108063751G>A, NR_046368.1:n.212C>T

Select item 138416861719.

rs1384168617 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 5:108728133 (GRCh38)
5:108063834 (GRCh37)
Canonical SPDI:: NC_000005.10:108728132:C:A
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000005.10:g.108728133C>A, NC_000005.9:g.108063834C>A, NR_046368.1:n.129G>T

Select item 137950277820.

rs1379502778 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 5:108727898 (GRCh38)
5:108063599 (GRCh37)
Canonical SPDI:: NC_000005.10:108727897:A:C,NC_000005.10:108727897:A:G
Gene:: LINC01023 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0./0 (Korea1K)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.108727898A>C, NC_000005.10:g.108727898A>G, NC_000005.9:g.108063599A>C, NC_000005.9:g.108063599A>G, NR_046368.1:n.364T>G, NR_046368.1:n.364T>C

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 127

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity