SNP Links for Protein (Select 543871463) - SNP

Links from Protein

Items: 1 to 20 of 358

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Select item 14844395681.

rs1484439568 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:135119782 (GRCh38)
9:138011628 (GRCh37)
Canonical SPDI:: NC_000009.12:135119781:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000223/1 (Estonian)
HGVS:: NC_000009.12:g.135119782C>T, NC_000009.11:g.138011628C>T, NM_014279.5:c.1008C>T, NM_014279.4:c.1008C>T, NM_001282611.2:c.1062C>T, NM_001282611.1:c.1062C>T, NM_001282612.1:c.981C>T

Select item 14815868982.

rs1481586898 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:135119591 (GRCh38)
9:138011437 (GRCh37)
Canonical SPDI:: NC_000009.12:135119590:T:G
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.135119591T>G, NC_000009.11:g.138011437T>G, NM_014279.5:c.817T>G, NM_014279.4:c.817T>G, NM_001282611.2:c.871T>G, NM_001282611.1:c.871T>G, NM_001282612.1:c.790T>G, NP_055094.1:p.Ser273Ala, NP_001269540.1:p.Ser291Ala, NP_001269541.1:p.Ser264Ala

Select item 14788260083.

rs1478826008 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:135120105 (GRCh38)
9:138011951 (GRCh37)
Canonical SPDI:: NC_000009.12:135120104:A:G
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.135120105A>G, NC_000009.11:g.138011951A>G, NM_014279.5:c.1331A>G, NM_014279.4:c.1331A>G, NM_001282611.2:c.1385A>G, NM_001282611.1:c.1385A>G, NM_001282612.1:c.1304A>G, NP_055094.1:p.Tyr444Cys, NP_001269540.1:p.Tyr462Cys, NP_001269541.1:p.Tyr435Cys

Select item 14756002614.

rs1475600261 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:135090328 (GRCh38)
9:137982174 (GRCh37)
Canonical SPDI:: NC_000009.12:135090327:G:A
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.135090328G>A, NC_000009.11:g.137982174G>A, NM_014279.5:c.230G>A, NM_014279.4:c.230G>A, NM_006334.4:c.230G>A, NM_006334.3:c.230G>A, NM_001282611.2:c.284G>A, NM_001282611.1:c.284G>A, NM_001282612.1:c.203G>A, NP_055094.1:p.Arg77Lys, NP_006325.1:p.Arg77Lys, NP_001269540.1:p.Arg95Lys, NP_001269541.1:p.Arg68Lys

Select item 14738695485.

rs1473869548 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:135095986 (GRCh38)
9:137987832 (GRCh37)
Canonical SPDI:: NC_000009.12:135095985:G:C
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000009/1 (GnomAD)
HGVS:: NC_000009.12:g.135095986G>C, NC_000009.11:g.137987832G>C, NM_014279.5:c.369G>C, NM_014279.4:c.369G>C, NM_006334.4:c.369G>C, NM_006334.3:c.369G>C, NM_001282611.2:c.423G>C, NM_001282611.1:c.423G>C, NM_001282612.1:c.342G>C, NP_055094.1:p.Glu123Asp, NP_006325.1:p.Glu123Asp, NP_001269540.1:p.Glu141Asp, NP_001269541.1:p.Glu114Asp

Select item 14700132036.

rs1470013203 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:135098295 (GRCh38)
9:137990141 (GRCh37)
Canonical SPDI:: NC_000009.12:135098294:G:A
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,downstream_transcript_variant,genic_downstream_transcript_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_000009.12:g.135098295G>A, NC_000009.11:g.137990141G>A, NM_014279.5:c.412G>A, NM_014279.4:c.412G>A, NM_001282611.2:c.466G>A, NM_001282611.1:c.466G>A, NM_001282612.1:c.385G>A, NP_055094.1:p.Ala138Thr, NP_001269540.1:p.Ala156Thr, NP_001269541.1:p.Ala129Thr

Select item 14696173207.

rs1469617320 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:135119845 (GRCh38)
9:138011691 (GRCh37)
Canonical SPDI:: NC_000009.12:135119844:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.135119845C>T, NC_000009.11:g.138011691C>T, NM_014279.5:c.1071C>T, NM_014279.4:c.1071C>T, NM_001282611.2:c.1125C>T, NM_001282611.1:c.1125C>T, NM_001282612.1:c.1044C>T

Select item 14668940508.

rs1466894050 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 9:135090239 (GRCh38)
9:137982085 (GRCh37)
Canonical SPDI:: NC_000009.12:135090238:T:G
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000009.12:g.135090239T>G, NC_000009.11:g.137982085T>G, NM_014279.5:c.141T>G, NM_014279.4:c.141T>G, NM_006334.4:c.141T>G, NM_006334.3:c.141T>G, NM_001282611.2:c.195T>G, NM_001282611.1:c.195T>G, NM_001282612.1:c.114T>G

Select item 14647564489.

rs1464756448 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:135088007 (GRCh38)
9:137979853 (GRCh37)
Canonical SPDI:: NC_000009.12:135088006:C:G
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.135088007C>G, NC_000009.11:g.137979853C>G, NM_001282611.2:c.18C>G, NM_001282611.1:c.18C>G

Select item 146455407010.

rs1464554070 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:135119659 (GRCh38)
9:138011505 (GRCh37)
Canonical SPDI:: NC_000009.12:135119658:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.135119659C>T, NC_000009.11:g.138011505C>T, NM_014279.5:c.885C>T, NM_014279.4:c.885C>T, NM_001282611.2:c.939C>T, NM_001282611.1:c.939C>T, NM_001282612.1:c.858C>T

Select item 146074158411.

rs1460741584 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:135120128 (GRCh38)
9:138011974 (GRCh37)
Canonical SPDI:: NC_000009.12:135120127:A:G
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.135120128A>G, NC_000009.11:g.138011974A>G, NM_014279.5:c.1354A>G, NM_014279.4:c.1354A>G, NM_001282611.2:c.1408A>G, NM_001282611.1:c.1408A>G, NM_001282612.1:c.1327A>G, NP_055094.1:p.Ile452Val, NP_001269540.1:p.Ile470Val, NP_001269541.1:p.Ile443Val

Select item 145687836212.

rs1456878362 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:135090336 (GRCh38)
9:137982182 (GRCh37)
Canonical SPDI:: NC_000009.12:135090335:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.135090336C>T, NC_000009.11:g.137982182C>T, NM_014279.5:c.238C>T, NM_014279.4:c.238C>T, NM_006334.4:c.238C>T, NM_006334.3:c.238C>T, NM_001282611.2:c.292C>T, NM_001282611.1:c.292C>T, NM_001282612.1:c.211C>T

Select item 145418641813.

rs1454186418 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:135119902 (GRCh38)
9:138011748 (GRCh37)
Canonical SPDI:: NC_000009.12:135119901:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.135119902C>T, NC_000009.11:g.138011748C>T, NM_014279.5:c.1128C>T, NM_014279.4:c.1128C>T, NM_001282611.2:c.1182C>T, NM_001282611.1:c.1182C>T, NM_001282612.1:c.1101C>T

Select item 144827787714.

rs1448277877 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:135088102 (GRCh38)
9:137979948 (GRCh37)
Canonical SPDI:: NC_000009.12:135088101:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.135088102C>T, NC_000009.11:g.137979948C>T, NM_001282611.2:c.113C>T, NM_001282611.1:c.113C>T, NP_001269540.1:p.Ser38Leu

Select item 144399492815.

rs1443994928 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:135120169 (GRCh38)
9:138012015 (GRCh37)
Canonical SPDI:: NC_000009.12:135120168:C:A,NC_000009.12:135120168:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00014/2 (TOMMO)
T=0.00055/1 (Korea1K)
HGVS:: NC_000009.12:g.135120169C>A, NC_000009.12:g.135120169C>T, NC_000009.11:g.138012015C>A, NC_000009.11:g.138012015C>T, NM_014279.5:c.1395C>A, NM_014279.5:c.1395C>T, NM_014279.4:c.1395C>A, NM_014279.4:c.1395C>T, NM_001282611.2:c.1449C>A, NM_001282611.2:c.1449C>T, NM_001282611.1:c.1449C>A, NM_001282611.1:c.1449C>T, NM_001282612.1:c.1368C>A, NM_001282612.1:c.1368C>T, NP_055094.1:p.Asp465Glu, NP_001269540.1:p.Asp483Glu, NP_001269541.1:p.Asp456Glu

Select item 143797458916.

rs1437974589 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:135088120 (GRCh38)
9:137979966 (GRCh37)
Canonical SPDI:: NC_000009.12:135088119:C:A,NC_000009.12:135088119:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000011/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.135088120C>A, NC_000009.12:g.135088120C>T, NC_000009.11:g.137979966C>A, NC_000009.11:g.137979966C>T, NM_001282611.2:c.131C>A, NM_001282611.2:c.131C>T, NM_001282611.1:c.131C>A, NM_001282611.1:c.131C>T, NP_001269540.1:p.Thr44Lys, NP_001269540.1:p.Thr44Met

Select item 143508778217.

rs1435087782 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:135095866 (GRCh38)
9:137987712 (GRCh37)
Canonical SPDI:: NC_000009.12:135095865:G:T
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.135095866G>T, NC_000009.11:g.137987712G>T, NM_014279.5:c.249G>T, NM_014279.4:c.249G>T, NM_006334.4:c.249G>T, NM_006334.3:c.249G>T, NM_001282611.2:c.303G>T, NM_001282611.1:c.303G>T, NM_001282612.1:c.222G>T

Select item 143270077118.

rs1432700771 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:135090220 (GRCh38)
9:137982066 (GRCh37)
Canonical SPDI:: NC_000009.12:135090219:G:A,NC_000009.12:135090219:G:C
Gene:: OLFM1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.135090220G>A, NC_000009.12:g.135090220G>C, NC_000009.11:g.137982066G>A, NC_000009.11:g.137982066G>C, NM_014279.5:c.122G>A, NM_014279.5:c.122G>C, NM_014279.4:c.122G>A, NM_014279.4:c.122G>C, NM_006334.4:c.122G>A, NM_006334.4:c.122G>C, NM_006334.3:c.122G>A, NM_006334.3:c.122G>C, NM_001282611.2:c.176G>A, NM_001282611.2:c.176G>C, NM_001282611.1:c.176G>A, NM_001282611.1:c.176G>C, NM_001282612.1:c.95G>A, NM_001282612.1:c.95G>C, NP_055094.1:p.Ser41Asn, NP_055094.1:p.Ser41Thr, NP_006325.1:p.Ser41Asn, NP_006325.1:p.Ser41Thr, NP_001269540.1:p.Ser59Asn, NP_001269540.1:p.Ser59Thr, NP_001269541.1:p.Ser32Asn, NP_001269541.1:p.Ser32Thr

Select item 142746247619.

rs1427462476 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:135119602 (GRCh38)
9:138011448 (GRCh37)
Canonical SPDI:: NC_000009.12:135119601:C:A,NC_000009.12:135119601:C:T
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.135119602C>A, NC_000009.12:g.135119602C>T, NC_000009.11:g.138011448C>A, NC_000009.11:g.138011448C>T, NM_014279.5:c.828C>A, NM_014279.5:c.828C>T, NM_014279.4:c.828C>A, NM_014279.4:c.828C>T, NM_001282611.2:c.882C>A, NM_001282611.2:c.882C>T, NM_001282611.1:c.882C>A, NM_001282611.1:c.882C>T, NM_001282612.1:c.801C>A, NM_001282612.1:c.801C>T

Select item 142740917220.

rs1427409172 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:135119905 (GRCh38)
9:138011751 (GRCh37)
Canonical SPDI:: NC_000009.12:135119904:G:A
Gene:: OLFM1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
A=0.000019/5 (TOPMED)
HGVS:: NC_000009.12:g.135119905G>A, NC_000009.11:g.138011751G>A, NM_014279.5:c.1131G>A, NM_014279.4:c.1131G>A, NM_001282611.2:c.1185G>A, NM_001282611.1:c.1185G>A, NM_001282612.1:c.1104G>A

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