SNP Links for Protein (Select 52352805) - SNP

Links from Protein

Items: 1 to 20 of 336

<< First< Prev

Page of 17

Next >Last >>

Select item 14904977041.

rs1490497704 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:26039814 (GRCh38)
1:26366305 (GRCh37)
Canonical SPDI:: NC_000001.11:26039813:C:A,NC_000001.11:26039813:C:T
Gene:: SLC30A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26039814C>A, NC_000001.11:g.26039814C>T, NC_000001.10:g.26366305C>A, NC_000001.10:g.26366305C>T, NG_042808.1:g.11325G>T, NG_042808.1:g.11325G>A, NM_032513.5:c.789G>T, NM_032513.5:c.789G>A, NM_032513.4:c.789G>T, NM_032513.4:c.789G>A, NM_032513.3:c.789G>T, NM_032513.3:c.789G>A, NM_001004434.3:c.936G>T, NM_001004434.3:c.936G>A, NM_001004434.2:c.936G>T, NM_001004434.2:c.936G>A, NM_001004434.1:c.936G>T, NM_001004434.1:c.936G>A

Select item 14888793112.

rs1488879311 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:26044336 (GRCh38)
1:26370827 (GRCh37)
Canonical SPDI:: NC_000001.11:26044335:G:T
Gene:: SLC30A2 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.26044336G>T, NC_000001.10:g.26370827G>T, NG_042808.1:g.6803C>A, NM_001004434.3:c.380C>A, NM_001004434.2:c.380C>A, NM_001004434.1:c.380C>A, NP_001004434.1:p.Pro127Gln

Select item 14869338263.

rs1486933826 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:26039184 (GRCh38)
1:26365675 (GRCh37)
Canonical SPDI:: NC_000001.11:26039183:C:T
Gene:: SLC30A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.26039184C>T, NC_000001.10:g.26365675C>T, NG_042808.1:g.11955G>A, NM_032513.5:c.948G>A, NM_032513.4:c.948G>A, NM_032513.3:c.948G>A, NM_001004434.3:c.1095G>A, NM_001004434.2:c.1095G>A, NM_001004434.1:c.1095G>A

Select item 14859482294.

rs1485948229 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:26039908 (GRCh38)
1:26366399 (GRCh37)
Canonical SPDI:: NC_000001.11:26039907:G:A
Gene:: SLC30A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26039908G>A, NC_000001.10:g.26366399G>A, NG_042808.1:g.11231C>T, NM_032513.5:c.695C>T, NM_032513.4:c.695C>T, NM_032513.3:c.695C>T, NM_001004434.3:c.842C>T, NM_001004434.2:c.842C>T, NM_001004434.1:c.842C>T, NP_115902.1:p.Thr232Ile, NP_001004434.1:p.Thr281Ile

Select item 14858839195.

rs1485883919 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:26039289 (GRCh38)
1:26365780 (GRCh37)
Canonical SPDI:: NC_000001.11:26039288:G:A
Gene:: SLC30A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.26039289G>A, NC_000001.10:g.26365780G>A, NG_042808.1:g.11850C>T, NM_032513.5:c.843C>T, NM_032513.4:c.843C>T, NM_032513.3:c.843C>T, NM_001004434.3:c.990C>T, NM_001004434.2:c.990C>T, NM_001004434.1:c.990C>T

Select item 14853586396.

rs1485358639 [Homo sapiens]

Variant type:: DEL
Alleles:: G>- [Show Flanks]
Chromosome:: 1:26042618 (GRCh38)
1:26369109 (GRCh37)
Canonical SPDI:: NC_000001.11:26042617:G:
Gene:: SLC30A2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.26042618del, NC_000001.10:g.26369109del, NG_042808.1:g.8521del, NM_032513.5:c.516del, NM_032513.4:c.516del, NM_032513.3:c.516del, NM_001004434.3:c.663del, NM_001004434.2:c.663del, NM_001004434.1:c.663del, NP_115902.1:p.Phe172fs, NP_001004434.1:p.Phe221fs

Select item 14849758737.

rs1484975873 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:26042590 (GRCh38)
1:26369081 (GRCh37)
Canonical SPDI:: NC_000001.11:26042589:T:C
Gene:: SLC30A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26042590T>C, NC_000001.10:g.26369081T>C, NG_042808.1:g.8549A>G, NM_032513.5:c.544A>G, NM_032513.4:c.544A>G, NM_032513.3:c.544A>G, NM_001004434.3:c.691A>G, NM_001004434.2:c.691A>G, NM_001004434.1:c.691A>G, NP_115902.1:p.Ser182Gly, NP_001004434.1:p.Ser231Gly

Select item 14839109788.

rs1483910978 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGT>- [Show Flanks]
Chromosome:: 1:26042653 (GRCh38)
1:26369144 (GRCh37)
Canonical SPDI:: NC_000001.11:26042651:TGGT:T
Gene:: SLC30A2 (Varview)
Functional Consequence:: inframe_indel,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26042653_26042655del, NC_000001.10:g.26369144_26369146del, NG_042808.1:g.8485_8487del, NM_032513.5:c.480_482del, NM_032513.4:c.480_482del, NM_032513.3:c.480_482del, NM_001004434.3:c.627_629del, NM_001004434.2:c.627_629del, NM_001004434.1:c.627_629del, NP_115902.1:p.Asn160_Gln161delinsLys, NP_001004434.1:p.Asn209_Gln210delinsLys

Select item 14824931049.

rs1482493104 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:26045109 (GRCh38)
1:26371600 (GRCh37)
Canonical SPDI:: NC_000001.11:26045108:G:A
Gene:: SLC30A2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26045109G>A, NC_000001.10:g.26371600G>A, NG_042808.1:g.6030C>T, NM_032513.5:c.159C>T, NM_032513.4:c.159C>T, NM_032513.3:c.159C>T, NM_001004434.3:c.159C>T, NM_001004434.2:c.159C>T, NM_001004434.1:c.159C>T

Select item 148190206810.

rs1481902068 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:26043435 (GRCh38)
1:26369926 (GRCh37)
Canonical SPDI:: NC_000001.11:26043434:G:T
Gene:: SLC30A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.26043435G>T, NC_000001.10:g.26369926G>T, NG_042808.1:g.7704C>A, NM_032513.5:c.388C>A, NM_032513.4:c.388C>A, NM_032513.3:c.388C>A, NM_001004434.3:c.535C>A, NM_001004434.2:c.535C>A, NM_001004434.1:c.535C>A, NP_115902.1:p.Leu130Met, NP_001004434.1:p.Leu179Met

Select item 147928983611.

rs1479289836 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:26045892 (GRCh38)
1:26372383 (GRCh37)
Canonical SPDI:: NC_000001.11:26045891:T:G
Gene:: SLC30A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26045892T>G, NC_000001.10:g.26372383T>G, NG_042808.1:g.5247A>C, NM_032513.5:c.5A>C, NM_032513.4:c.5A>C, NM_032513.3:c.5A>C, NM_001004434.3:c.5A>C, NM_001004434.2:c.5A>C, NM_001004434.1:c.5A>C, NP_115902.1:p.Glu2Ala, NP_001004434.1:p.Glu2Ala

Select item 147710926712.

rs1477109267 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:26039815 (GRCh38)
1:26366306 (GRCh37)
Canonical SPDI:: NC_000001.11:26039814:G:A
Gene:: SLC30A2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26039815G>A, NC_000001.10:g.26366306G>A, NG_042808.1:g.11324C>T, NM_032513.5:c.788C>T, NM_032513.4:c.788C>T, NM_032513.3:c.788C>T, NM_001004434.3:c.935C>T, NM_001004434.2:c.935C>T, NM_001004434.1:c.935C>T, NP_115902.1:p.Thr263Met, NP_001004434.1:p.Thr312Met

Select item 147252016613.

rs1472520166 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:26043439 (GRCh38)
1:26369930 (GRCh37)
Canonical SPDI:: NC_000001.11:26043438:G:A
Gene:: SLC30A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26043439G>A, NC_000001.10:g.26369930G>A, NG_042808.1:g.7700C>T, NM_032513.5:c.384C>T, NM_032513.4:c.384C>T, NM_032513.3:c.384C>T, NM_001004434.3:c.531C>T, NM_001004434.2:c.531C>T, NM_001004434.1:c.531C>T

Select item 147194333514.

rs1471943335 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:26044391 (GRCh38)
1:26370882 (GRCh37)
Canonical SPDI:: NC_000001.11:26044390:T:C
Gene:: SLC30A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26044391T>C, NC_000001.10:g.26370882T>C, NG_042808.1:g.6748A>G, NM_001004434.3:c.325A>G, NM_001004434.2:c.325A>G, NM_001004434.1:c.325A>G, NP_001004434.1:p.Thr109Ala

Select item 147160277815.

rs1471602778 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:26045214 (GRCh38)
1:26371705 (GRCh37)
Canonical SPDI:: NC_000001.11:26045213:T:C
Gene:: SLC30A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26045214T>C, NC_000001.10:g.26371705T>C, NG_042808.1:g.5925A>G, NM_032513.5:c.54A>G, NM_032513.4:c.54A>G, NM_032513.3:c.54A>G, NM_001004434.3:c.54A>G, NM_001004434.2:c.54A>G, NM_001004434.1:c.54A>G

Select item 147101565216.

rs1471015652 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:26045170 (GRCh38)
1:26371661 (GRCh37)
Canonical SPDI:: NC_000001.11:26045169:A:C
Gene:: SLC30A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26045170A>C, NC_000001.10:g.26371661A>C, NG_042808.1:g.5969T>G, NM_032513.5:c.98T>G, NM_032513.4:c.98T>G, NM_032513.3:c.98T>G, NM_001004434.3:c.98T>G, NM_001004434.2:c.98T>G, NM_001004434.1:c.98T>G, NP_115902.1:p.Leu33Arg, NP_001004434.1:p.Leu33Arg

Select item 147006664917.

rs1470066649 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:26041791 (GRCh38)
1:26368282 (GRCh37)
Canonical SPDI:: NC_000001.11:26041790:A:G
Gene:: SLC30A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26041791A>G, NC_000001.10:g.26368282A>G, NG_042808.1:g.9348T>C, NM_032513.5:c.600T>C, NM_032513.4:c.600T>C, NM_032513.3:c.600T>C, NM_001004434.3:c.747T>C, NM_001004434.2:c.747T>C, NM_001004434.1:c.747T>C

Select item 146759713518.

rs1467597135 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:26042684 (GRCh38)
1:26369175 (GRCh37)
Canonical SPDI:: NC_000001.11:26042683:A:G
Gene:: SLC30A2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26042684A>G, NC_000001.10:g.26369175A>G, NG_042808.1:g.8455T>C, NM_032513.5:c.450T>C, NM_032513.4:c.450T>C, NM_032513.3:c.450T>C, NM_001004434.3:c.597T>C, NM_001004434.2:c.597T>C, NM_001004434.1:c.597T>C

Select item 146513852019.

rs1465138520 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:26045140 (GRCh38)
1:26371631 (GRCh37)
Canonical SPDI:: NC_000001.11:26045139:A:G
Gene:: SLC30A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000001.11:g.26045140A>G, NC_000001.10:g.26371631A>G, NG_042808.1:g.5999T>C, NM_032513.5:c.128T>C, NM_032513.4:c.128T>C, NM_032513.3:c.128T>C, NM_001004434.3:c.128T>C, NM_001004434.2:c.128T>C, NM_001004434.1:c.128T>C, NP_115902.1:p.Ile43Thr, NP_001004434.1:p.Ile43Thr

Select item 146238293220.

rs1462382932 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:26043479 (GRCh38)
1:26369970 (GRCh37)
Canonical SPDI:: NC_000001.11:26043478:T:G
Gene:: SLC30A2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000084/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26043479T>G, NC_000001.10:g.26369970T>G, NG_042808.1:g.7660A>C, NM_032513.5:c.344A>C, NM_032513.4:c.344A>C, NM_032513.3:c.344A>C, NM_001004434.3:c.491A>C, NM_001004434.2:c.491A>C, NM_001004434.1:c.491A>C, NP_115902.1:p.Glu115Ala, NP_001004434.1:p.Glu164Ala

<< First< Prev

Page of 17

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 336

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity