SNP Links for Gene (Select 124220) - SNP

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Select item 14884377161.

rs1488437716 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2829522 (GRCh38)
16:2879523 (GRCh37)
Canonical SPDI:: NC_000016.10:2829521:G:A
Gene:: ZG16B (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.2829522G>A, NC_000016.9:g.2879523G>A, NW_013171812.1:g.8987G>A

Select item 14881459652.

rs1488145965 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:2830827 (GRCh38)
16:2880828 (GRCh37)
Canonical SPDI:: NC_000016.10:2830826:C:G
Gene:: ZG16B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (GnomAD)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2830827C>G, NC_000016.9:g.2880828C>G, NW_013171812.1:g.10292C>G

Select item 14879541583.

rs1487954158 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:2832343 (GRCh38)
16:2882344 (GRCh37)
Canonical SPDI:: NC_000016.10:2832342:A:G
Gene:: ZG16B (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.2832343A>G, NC_000016.9:g.2882344A>G, NW_013171812.1:g.11808A>G

Select item 14869605864.

rs1486960586 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:2830480 (GRCh38)
16:2880481 (GRCh37)
Canonical SPDI:: NC_000016.10:2830479:C:G
Gene:: ZG16B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.2830480C>G, NC_000016.9:g.2880481C>G, NW_013171812.1:g.9945C>G, NM_145252.3:c.39C>G, NM_145252.2:c.147C>G

Select item 14866838895.

rs1486683889 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:2830441 (GRCh38)
16:2880442 (GRCh37)
Canonical SPDI:: NC_000016.10:2830440:C:T
Gene:: ZG16B (Varview)
Functional Consequence:: 5_prime_UTR_variant
HGVS:: NC_000016.10:g.2830441C>T, NC_000016.9:g.2880442C>T, NW_013171812.1:g.9906C>T, NM_145252.3:c.-1C>T, NM_145252.2:c.108C>T

Select item 14866339566.

rs1486633956 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2832097 (GRCh38)
16:2882098 (GRCh37)
Canonical SPDI:: NC_000016.10:2832096:G:A
Gene:: ZG16B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
A=0.000016/4 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
A=0.000684/2 (KOREAN)
HGVS:: NC_000016.10:g.2832097G>A, NC_000016.9:g.2882098G>A, NW_013171812.1:g.11562G>A, NM_145252.3:c.457G>A, NM_145252.2:c.565G>A, NP_660295.3:p.Glu153Lys

Select item 14864460587.

rs1486446058 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:2829329 (GRCh38)
16:2879330 (GRCh37)
Canonical SPDI:: NC_000016.10:2829328:C:A
Gene:: ZG16B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.2829329C>A, NC_000016.9:g.2879330C>A, NW_013171812.1:g.8794C>A

Select item 14864310978.

rs1486431097 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 16:2831621 (GRCh38)
16:2881622 (GRCh37)
Canonical SPDI:: NC_000016.10:2831620:A:T
Gene:: ZG16B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000016.10:g.2831621A>T, NC_000016.9:g.2881622A>T, NW_013171812.1:g.11086A>T

Select item 14854583719.

rs1485458371 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:2828534 (GRCh38)
16:2878535 (GRCh37)
Canonical SPDI:: NC_000016.10:2828533:A:C
Gene:: ZG16B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.2828534A>C, NC_000016.9:g.2878535A>C, NW_013171812.1:g.7999A>C

Select item 148369671310.

rs1483696713 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:2830035 (GRCh38)
16:2880036 (GRCh37)
Canonical SPDI:: NC_000016.10:2830034:A:C
Gene:: ZG16B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.2830035A>C, NC_000016.9:g.2880036A>C, NW_013171812.1:g.9500A>C

Select item 148283677511.

rs1482836775 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:2832042 (GRCh38)
16:2882043 (GRCh37)
Canonical SPDI:: NC_000016.10:2832041:G:T
Gene:: ZG16B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.2832042G>T, NC_000016.9:g.2882043G>T, NW_013171812.1:g.11507G>T, NM_145252.3:c.402G>T, NM_145252.2:c.510G>T, NP_660295.3:p.Gln134His

Select item 148149425612.

rs1481494256 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:2831584 (GRCh38)
16:2881585 (GRCh37)
Canonical SPDI:: NC_000016.10:2831583:A:G
Gene:: ZG16B (Varview)
Functional Consequence:: intron_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_000016.10:g.2831584A>G, NC_000016.9:g.2881585A>G, NW_013171812.1:g.11049A>G

Select item 147858865413.

rs1478588654 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:2830401 (GRCh38)
16:2880402 (GRCh37)
Canonical SPDI:: NC_000016.10:2830400:T:A
Gene:: ZG16B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.2830401T>A, NC_000016.9:g.2880402T>A, NW_013171812.1:g.9866T>A

Select item 147790965014.

rs1477909650 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2828259 (GRCh38)
16:2878260 (GRCh37)
Canonical SPDI:: NC_000016.10:2828258:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000016.10:g.2828259G>A, NC_000016.9:g.2878260G>A, NW_013171812.1:g.7724G>A

Select item 147787531315.

rs1477875313 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:2829076 (GRCh38)
16:2879077 (GRCh37)
Canonical SPDI:: NC_000016.10:2829075:C:T
Gene:: ZG16B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000342/1 (KOREAN)
HGVS:: NC_000016.10:g.2829076C>T, NC_000016.9:g.2879077C>T, NW_013171812.1:g.8541C>T

Select item 147783561616.

rs1477835616 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2829354 (GRCh38)
16:2879355 (GRCh37)
Canonical SPDI:: NC_000016.10:2829353:G:A
Gene:: ZG16B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000016.10:g.2829354G>A, NC_000016.9:g.2879355G>A, NW_013171812.1:g.8819G>A

Select item 147780701617.

rs1477807016 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:2830207 (GRCh38)
16:2880208 (GRCh37)
Canonical SPDI:: NC_000016.10:2830206:C:A
Gene:: ZG16B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.2830207C>A, NC_000016.9:g.2880208C>A, NW_013171812.1:g.9672C>A, NM_145252.2:c.-41C>A

Select item 147618038318.

rs1476180383 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:2832558 (GRCh38)
16:2882559 (GRCh37)
Canonical SPDI:: NC_000016.10:2832557:C:T
Gene:: ZG16B (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000023/6 (TOPMED)
T=0.000024/3 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000016.10:g.2832558C>T, NC_000016.9:g.2882559C>T, NW_013171812.1:g.12023C>T

Select item 147599723619.

rs1475997236 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:2831695 (GRCh38)
16:2881696 (GRCh37)
Canonical SPDI:: NC_000016.10:2831694:T:C
Gene:: ZG16B (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.2831695T>C, NC_000016.9:g.2881696T>C, NW_013171812.1:g.11160T>C

Select item 147489514620.

rs1474895146 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 16:2830046 (GRCh38)
16:2880047 (GRCh37)
Canonical SPDI:: NC_000016.10:2830045:G:A,NC_000016.10:2830045:G:C
Gene:: ZG16B (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.2830046G>A, NC_000016.10:g.2830046G>C, NC_000016.9:g.2880047G>A, NC_000016.9:g.2880047G>C, NW_013171812.1:g.9511G>A, NW_013171812.1:g.9511G>C

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