SNP Links for Protein (Select 924966810) - SNP

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Links from Protein

Items: 1 to 20 of 164

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Select item 14892974271.

rs1489297427 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:18798015 (GRCh38)
16:18809337 (GRCh37)
Canonical SPDI:: NC_000016.10:18798014:A:G
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
HGVS:: NC_000016.10:g.18798015A>G, NC_000016.9:g.18809337A>G, NG_042860.1:g.8664T>C, NM_015161.3:c.200T>C, NM_015161.2:c.200T>C, NM_015161.1:c.200T>C, NM_001313858.1:c.113T>C, NP_055976.1:p.Leu67Pro, NP_001300787.1:p.Leu38Pro

Select item 14858385712.

rs1485838571 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:18795466 (GRCh38)
16:18806788 (GRCh37)
Canonical SPDI:: NC_000016.10:18795465:T:G
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000016.10:g.18795466T>G, NC_000016.9:g.18806788T>G, NG_042860.1:g.11213A>C, NM_015161.3:c.406A>C, NM_015161.2:c.406A>C, NM_015161.1:c.406A>C, NM_001313858.1:c.319A>C, NP_055976.1:p.Met136Leu, NP_001300787.1:p.Met107Leu

Select item 14829057993.

rs1482905799 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 16:18793268 (GRCh38)
16:18804590 (GRCh37)
Canonical SPDI:: NC_000016.10:18793267:T:C,NC_000016.10:18793267:T:G
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.18793268T>C, NC_000016.10:g.18793268T>G, NC_000016.9:g.18804590T>C, NC_000016.9:g.18804590T>G, NG_042860.1:g.13411A>G, NG_042860.1:g.13411A>C, NM_015161.3:c.596A>G, NM_015161.3:c.596A>C, NM_015161.2:c.596A>G, NM_015161.2:c.596A>C, NM_015161.1:c.596A>G, NM_015161.1:c.596A>C, NM_001313858.1:c.509A>G, NM_001313858.1:c.509A>C, NP_055976.1:p.Glu199Gly, NP_055976.1:p.Glu199Ala, NP_001300787.1:p.Glu170Gly, NP_001300787.1:p.Glu170Ala

Select item 14761509404.

rs1476150940 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 16:18793296 (GRCh38)
16:18804618 (GRCh37)
Canonical SPDI:: NC_000016.10:18793295:CCC:CC
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0.000071/1 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.18793298del, NC_000016.9:g.18804620del, NG_042860.1:g.13383del, NM_015161.3:c.568del, NM_015161.2:c.568del, NM_015161.1:c.568del, NM_001313858.1:c.481del, NP_055976.1:p.Glu190fs, NP_001300787.1:p.Glu161fs

Select item 14742216535.

rs1474221653 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:18798035 (GRCh38)
16:18809357 (GRCh37)
Canonical SPDI:: NC_000016.10:18798034:G:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000016.10:g.18798035G>A, NC_000016.9:g.18809357G>A, NG_042860.1:g.8644C>T, NM_015161.3:c.180C>T, NM_015161.2:c.180C>T, NM_015161.1:c.180C>T, NM_001313858.1:c.93C>T

Select item 14732644006.

rs1473264400 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:18793355 (GRCh38)
16:18804677 (GRCh37)
Canonical SPDI:: NC_000016.10:18793354:A:G
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000016.10:g.18793355A>G, NC_000016.9:g.18804677A>G, NG_042860.1:g.13324T>C, NM_015161.3:c.509T>C, NM_015161.2:c.509T>C, NM_015161.1:c.509T>C, NM_001313858.1:c.422T>C, NP_055976.1:p.Leu170Ser, NP_001300787.1:p.Leu141Ser

Select item 14613373287.

rs1461337328 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:18794652 (GRCh38)
16:18805974 (GRCh37)
Canonical SPDI:: NC_000016.10:18794651:G:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000012/3 (GnomAD_exomes)
A=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.18794652G>A, NC_000016.9:g.18805974G>A, NG_042860.1:g.12027C>T, NM_015161.3:c.440C>T, NM_015161.2:c.440C>T, NM_015161.1:c.440C>T, NM_001313858.1:c.353C>T, NP_055976.1:p.Ala147Val, NP_001300787.1:p.Ala118Val

Select item 14544106828.

rs1454410682 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:18795578 (GRCh38)
16:18806900 (GRCh37)
Canonical SPDI:: NC_000016.10:18795577:G:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.18795578G>A, NC_000016.9:g.18806900G>A, NG_042860.1:g.11101C>T, NM_015161.3:c.294C>T, NM_015161.2:c.294C>T, NM_015161.1:c.294C>T, NM_001313858.1:c.207C>T

Select item 14510132899.

rs1451013289 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:18795487 (GRCh38)
16:18806809 (GRCh37)
Canonical SPDI:: NC_000016.10:18795486:G:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.18795487G>A, NC_000016.9:g.18806809G>A, NG_042860.1:g.11192C>T, NM_015161.3:c.385C>T, NM_015161.2:c.385C>T, NM_015161.1:c.385C>T, NM_001313858.1:c.298C>T

Select item 145072989110.

rs1450729891 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:18798738 (GRCh38)
16:18810060 (GRCh37)
Canonical SPDI:: NC_000016.10:18798737:G:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.18798738G>A, NC_000016.9:g.18810060G>A, NG_042860.1:g.7941C>T, NM_015161.3:c.133C>T, NM_015161.2:c.133C>T, NM_015161.1:c.133C>T, NM_001313858.1:c.46C>T, NP_055976.1:p.Pro45Ser, NP_001300787.1:p.Pro16Ser

Select item 143542057711.

rs1435420577 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:18798750 (GRCh38)
16:18810072 (GRCh37)
Canonical SPDI:: NC_000016.10:18798749:T:C
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.000007/1 (GnomAD)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000016.10:g.18798750T>C, NC_000016.9:g.18810072T>C, NG_042860.1:g.7929A>G, NM_015161.3:c.121A>G, NM_015161.2:c.121A>G, NM_015161.1:c.121A>G, NM_001313858.1:c.34A>G, NP_055976.1:p.Arg41Gly, NP_001300787.1:p.Arg12Gly

Select item 143330283712.

rs1433302837 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:18795560 (GRCh38)
16:18806882 (GRCh37)
Canonical SPDI:: NC_000016.10:18795559:T:G
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.18795560T>G, NC_000016.9:g.18806882T>G, NG_042860.1:g.11119A>C, NM_015161.3:c.312A>C, NM_015161.2:c.312A>C, NM_015161.1:c.312A>C, NM_001313858.1:c.225A>C, NP_055976.1:p.Arg104Ser, NP_001300787.1:p.Arg75Ser

Select item 142832149013.

rs1428321490 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:18798759 (GRCh38)
16:18810081 (GRCh37)
Canonical SPDI:: NC_000016.10:18798758:G:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
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.18798759G>A, NC_000016.9:g.18810081G>A, NG_042860.1:g.7920C>T, NM_015161.3:c.112C>T, NM_015161.2:c.112C>T, NM_015161.1:c.112C>T, NM_001313858.1:c.25C>T, NP_055976.1:p.Arg38Ter, NP_001300787.1:p.Arg9Ter

Select item 142012893014.

rs1420128930 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:18794663 (GRCh38)
16:18805985 (GRCh37)
Canonical SPDI:: NC_000016.10:18794662:A:C
Gene:: ARL6IP1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000016.10:g.18794663A>C, NC_000016.9:g.18805985A>C, NG_042860.1:g.12016T>G, NM_015161.3:c.429T>G, NM_015161.2:c.429T>G, NM_015161.1:c.429T>G, NM_001313858.1:c.342T>G

Select item 141502208415.

rs1415022084 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:18795542 (GRCh38)
16:18806864 (GRCh37)
Canonical SPDI:: NC_000016.10:18795541:G:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.18795542G>A, NC_000016.9:g.18806864G>A, NG_042860.1:g.11137C>T, NM_015161.3:c.330C>T, NM_015161.2:c.330C>T, NM_015161.1:c.330C>T, NM_001313858.1:c.243C>T

Select item 141379488216.

rs1413794882 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:18794607 (GRCh38)
16:18805929 (GRCh37)
Canonical SPDI:: NC_000016.10:18794606:T:G
Gene:: ARL6IP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.18794607T>G, NC_000016.9:g.18805929T>G, NG_042860.1:g.12072A>C, NM_015161.3:c.485A>C, NM_015161.2:c.485A>C, NM_015161.1:c.485A>C, NM_001313858.1:c.398A>C, NP_055976.1:p.Tyr162Ser, NP_001300787.1:p.Tyr133Ser

Select item 140311180317.

rs1403111803 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:18798708 (GRCh38)
16:18810030 (GRCh37)
Canonical SPDI:: NC_000016.10:18798707:C:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.18798708C>A, NC_000016.9:g.18810030C>A, NG_042860.1:g.7971G>T, NM_015161.3:c.163G>T, NM_015161.2:c.163G>T, NM_015161.1:c.163G>T, NM_001313858.1:c.76G>T, NP_055976.1:p.Val55Leu, NP_001300787.1:p.Val26Leu

Select item 139430724718.

rs1394307247 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:18795515 (GRCh38)
16:18806837 (GRCh37)
Canonical SPDI:: NC_000016.10:18795514:A:G
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.18795515A>G, NC_000016.9:g.18806837A>G, NG_042860.1:g.11164T>C, NM_015161.3:c.357T>C, NM_015161.2:c.357T>C, NM_015161.1:c.357T>C, NM_001313858.1:c.270T>C

Select item 139281812519.

rs1392818125 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:18797982 (GRCh38)
16:18809304 (GRCh37)
Canonical SPDI:: NC_000016.10:18797981:C:A
Gene:: ARL6IP1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.18797982C>A, NC_000016.9:g.18809304C>A, NG_042860.1:g.8697G>T, NM_015161.3:c.233G>T, NM_015161.2:c.233G>T, NM_015161.1:c.233G>T, NM_001313858.1:c.146G>T, NP_055976.1:p.Cys78Phe, NP_001300787.1:p.Cys49Phe

Select item 139247314020.

rs1392473140 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:18798718 (GRCh38)
16:18810040 (GRCh37)
Canonical SPDI:: NC_000016.10:18798717:C:T
Gene:: ARL6IP1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.18798718C>T, NC_000016.9:g.18810040C>T, NG_042860.1:g.7961G>A, NM_015161.3:c.153G>A, NM_015161.2:c.153G>A, NM_015161.1:c.153G>A, NM_001313858.1:c.66G>A

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