SNP Links for Protein (Select 343478159) - SNP

Links from Protein

Items: 1 to 20 of 68

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Select item 14884899661.

rs1488489966 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:17987079 (GRCh38)
6:17987310 (GRCh37)
Canonical SPDI:: NC_000006.12:17987078:G:A
Gene:: KIF13A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000047/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.17987079G>A, NC_000006.11:g.17987310G>A, NG_029766.1:g.5545C>T, NM_022113.6:c.121C>T, NM_022113.5:c.121C>T, NM_001105568.4:c.121C>T, NM_001105568.3:c.121C>T, NM_001105568.2:c.121C>T, NM_001105566.3:c.121C>T, NM_001105566.2:c.121C>T, NM_001105567.3:c.121C>T, NM_001105567.2:c.121C>T, NM_001243423.2:c.121C>T, NM_001243423.1:c.121C>T, NP_071396.4:p.Pro41Ser, NP_001099038.1:p.Pro41Ser, NP_001099036.1:p.Pro41Ser, NP_001099037.1:p.Pro41Ser, NP_001230352.1:p.Pro41Ser

Select item 14623918702.

rs1462391870 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:17951401 (GRCh38)
6:17951632 (GRCh37)
Canonical SPDI:: NC_000006.12:17951400:A:G
Gene:: KIF13A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000051/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.17951401A>G, NC_000006.11:g.17951632A>G, NG_029766.1:g.41223T>C, NM_001243423.2:c.175T>C, NM_001243423.1:c.175T>C, NP_001230352.1:p.Ser59Pro

Select item 14378273513.

rs1437827351 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:17987448 (GRCh38)
6:17987679 (GRCh37)
Canonical SPDI:: NC_000006.12:17987447:C:T
Gene:: KIF13A (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_000006.12:g.17987448C>T, NC_000006.11:g.17987679C>T, NG_029766.1:g.5176G>A, NM_022113.6:c.16G>A, NM_022113.5:c.16G>A, NM_001105568.4:c.16G>A, NM_001105568.3:c.16G>A, NM_001105568.2:c.16G>A, NM_001105566.3:c.16G>A, NM_001105566.2:c.16G>A, NM_001105567.3:c.16G>A, NM_001105567.2:c.16G>A, NM_001243423.2:c.16G>A, NM_001243423.1:c.16G>A, NP_071396.4:p.Val6Ile, NP_001099038.1:p.Val6Ile, NP_001099036.1:p.Val6Ile, NP_001099037.1:p.Val6Ile, NP_001230352.1:p.Val6Ile

Select item 14120926404.

rs1412092640 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:17987409 (GRCh38)
6:17987640 (GRCh37)
Canonical SPDI:: NC_000006.12:17987408:C:T
Gene:: KIF13A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000006.12:g.17987409C>T, NC_000006.11:g.17987640C>T, NG_029766.1:g.5215G>A, NM_022113.6:c.55G>A, NM_022113.5:c.55G>A, NM_001105568.4:c.55G>A, NM_001105568.3:c.55G>A, NM_001105568.2:c.55G>A, NM_001105566.3:c.55G>A, NM_001105566.2:c.55G>A, NM_001105567.3:c.55G>A, NM_001105567.2:c.55G>A, NM_001243423.2:c.55G>A, NM_001243423.1:c.55G>A, NP_071396.4:p.Glu19Lys, NP_001099038.1:p.Glu19Lys, NP_001099036.1:p.Glu19Lys, NP_001099037.1:p.Glu19Lys, NP_001230352.1:p.Glu19Lys

Select item 14054112695.

rs1405411269 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:17987412 (GRCh38)
6:17987643 (GRCh37)
Canonical SPDI:: NC_000006.12:17987411:G:T
Gene:: KIF13A (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000006.12:g.17987412G>T, NC_000006.11:g.17987643G>T, NG_029766.1:g.5212C>A, NM_022113.6:c.52C>A, NM_022113.5:c.52C>A, NM_001105568.4:c.52C>A, NM_001105568.3:c.52C>A, NM_001105568.2:c.52C>A, NM_001105566.3:c.52C>A, NM_001105566.2:c.52C>A, NM_001105567.3:c.52C>A, NM_001105567.2:c.52C>A, NM_001243423.2:c.52C>A, NM_001243423.1:c.52C>A

Select item 14032349626.

rs1403234962 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:17951409 (GRCh38)
6:17951640 (GRCh37)
Canonical SPDI:: NC_000006.12:17951408:A:G
Gene:: KIF13A (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.0001/1 (ALFA)
HGVS:: NC_000006.12:g.17951409A>G, NC_000006.11:g.17951640A>G, NG_029766.1:g.41215T>C, NM_001243423.2:c.167T>C, NM_001243423.1:c.167T>C, NP_001230352.1:p.Ile56Thr

Select item 13986450247.

rs1398645024 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:17987092 (GRCh38)
6:17987323 (GRCh37)
Canonical SPDI:: NC_000006.12:17987091:G:T
Gene:: KIF13A (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000006.12:g.17987092G>T, NC_000006.11:g.17987323G>T, NG_029766.1:g.5532C>A, NM_022113.6:c.108C>A, NM_022113.5:c.108C>A, NM_001105568.4:c.108C>A, NM_001105568.3:c.108C>A, NM_001105568.2:c.108C>A, NM_001105566.3:c.108C>A, NM_001105566.2:c.108C>A, NM_001105567.3:c.108C>A, NM_001105567.2:c.108C>A, NM_001243423.2:c.108C>A, NM_001243423.1:c.108C>A

Select item 13938449408.

rs1393844940 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:17987114 (GRCh38)
6:17987345 (GRCh37)
Canonical SPDI:: NC_000006.12:17987113:T:A
Gene:: KIF13A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.17987114T>A, NC_000006.11:g.17987345T>A, NG_029766.1:g.5510A>T, NM_022113.6:c.86A>T, NM_022113.5:c.86A>T, NM_001105568.4:c.86A>T, NM_001105568.3:c.86A>T, NM_001105568.2:c.86A>T, NM_001105566.3:c.86A>T, NM_001105566.2:c.86A>T, NM_001105567.3:c.86A>T, NM_001105567.2:c.86A>T, NM_001243423.2:c.86A>T, NM_001243423.1:c.86A>T, NP_071396.4:p.Glu29Val, NP_001099038.1:p.Glu29Val, NP_001099036.1:p.Glu29Val, NP_001099037.1:p.Glu29Val, NP_001230352.1:p.Glu29Val

Select item 13856978169.

rs1385697816 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:17951370 (GRCh38)
6:17951601 (GRCh37)
Canonical SPDI:: NC_000006.12:17951369:A:G
Gene:: KIF13A (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
HGVS:: NC_000006.12:g.17951370A>G, NC_000006.11:g.17951601A>G, NG_029766.1:g.41254T>C, NM_001243423.2:c.206T>C, NM_001243423.1:c.206T>C, NP_001230352.1:p.Ile69Thr

Select item 138165311410.

rs1381653114 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:17951427 (GRCh38)
6:17951658 (GRCh37)
Canonical SPDI:: NC_000006.12:17951426:A:G
Gene:: KIF13A (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.17951427A>G, NC_000006.11:g.17951658A>G, NG_029766.1:g.41197T>C, NM_001243423.2:c.149T>C, NM_001243423.1:c.149T>C, NP_001230352.1:p.Leu50Pro

Select item 138106537611.

rs1381065376 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:17987453 (GRCh38)
6:17987684 (GRCh37)
Canonical SPDI:: NC_000006.12:17987452:G:T
Gene:: KIF13A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.17987453G>T, NC_000006.11:g.17987684G>T, NG_029766.1:g.5171C>A, NM_022113.6:c.11C>A, NM_022113.5:c.11C>A, NM_001105568.4:c.11C>A, NM_001105568.3:c.11C>A, NM_001105568.2:c.11C>A, NM_001105566.3:c.11C>A, NM_001105566.2:c.11C>A, NM_001105567.3:c.11C>A, NM_001105567.2:c.11C>A, NM_001243423.2:c.11C>A, NM_001243423.1:c.11C>A, NP_071396.4:p.Thr4Asn, NP_001099038.1:p.Thr4Asn, NP_001099036.1:p.Thr4Asn, NP_001099037.1:p.Thr4Asn, NP_001230352.1:p.Thr4Asn

Select item 137001783612.

rs1370017836 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:17951393 (GRCh38)
6:17951624 (GRCh37)
Canonical SPDI:: NC_000006.12:17951392:A:T
Gene:: KIF13A (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.17951393A>T, NC_000006.11:g.17951624A>T, NG_029766.1:g.41231T>A, NM_001243423.2:c.183T>A, NM_001243423.1:c.183T>A

Select item 136075742513.

rs1360757425 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 6:17951422 (GRCh38)
6:17951653 (GRCh37)
Canonical SPDI:: NC_000006.12:17951421:T:A
Gene:: KIF13A (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
HGVS:: NC_000006.12:g.17951422T>A, NC_000006.11:g.17951653T>A, NG_029766.1:g.41202A>T, NM_001243423.2:c.154A>T, NM_001243423.1:c.154A>T, NP_001230352.1:p.Thr52Ser

Select item 135622420214.

rs1356224202 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:17951400 (GRCh38)
6:17951631 (GRCh37)
Canonical SPDI:: NC_000006.12:17951399:G:A
Gene:: KIF13A (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.0001/1 (ALFA)
HGVS:: NC_000006.12:g.17951400G>A, NC_000006.11:g.17951631G>A, NG_029766.1:g.41224C>T, NM_001243423.2:c.176C>T, NM_001243423.1:c.176C>T, NP_001230352.1:p.Ser59Phe

Select item 133894185215.

rs1338941852 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:17987420 (GRCh38)
6:17987651 (GRCh37)
Canonical SPDI:: NC_000006.12:17987419:A:T
Gene:: KIF13A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.17987420A>T, NC_000006.11:g.17987651A>T, NG_029766.1:g.5204T>A, NM_022113.6:c.44T>A, NM_022113.5:c.44T>A, NM_001105568.4:c.44T>A, NM_001105568.3:c.44T>A, NM_001105568.2:c.44T>A, NM_001105566.3:c.44T>A, NM_001105566.2:c.44T>A, NM_001105567.3:c.44T>A, NM_001105567.2:c.44T>A, NM_001243423.2:c.44T>A, NM_001243423.1:c.44T>A, NP_071396.4:p.Met15Lys, NP_001099038.1:p.Met15Lys, NP_001099036.1:p.Met15Lys, NP_001099037.1:p.Met15Lys, NP_001230352.1:p.Met15Lys

Select item 133710321516.

rs1337103215 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:17987098 (GRCh38)
6:17987329 (GRCh37)
Canonical SPDI:: NC_000006.12:17987097:T:C
Gene:: KIF13A (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000006.12:g.17987098T>C, NC_000006.11:g.17987329T>C, NG_029766.1:g.5526A>G, NM_022113.6:c.102A>G, NM_022113.5:c.102A>G, NM_001105568.4:c.102A>G, NM_001105568.3:c.102A>G, NM_001105568.2:c.102A>G, NM_001105566.3:c.102A>G, NM_001105566.2:c.102A>G, NM_001105567.3:c.102A>G, NM_001105567.2:c.102A>G, NM_001243423.2:c.102A>G, NM_001243423.1:c.102A>G

Select item 133554245917.

rs1335542459 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:17951406 (GRCh38)
6:17951637 (GRCh37)
Canonical SPDI:: NC_000006.12:17951405:G:C
Gene:: KIF13A (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000051/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000156/1 (1000Genomes)
HGVS:: NC_000006.12:g.17951406G>C, NC_000006.11:g.17951637G>C, NG_029766.1:g.41218C>G, NM_001243423.2:c.170C>G, NM_001243423.1:c.170C>G, NP_001230352.1:p.Ser57Cys

Select item 132966827718.

rs1329668277 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:17987411 (GRCh38)
6:17987642 (GRCh37)
Canonical SPDI:: NC_000006.12:17987410:C:T
Gene:: KIF13A (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000006.12:g.17987411C>T, NC_000006.11:g.17987642C>T, NG_029766.1:g.5213G>A, NM_022113.6:c.53G>A, NM_022113.5:c.53G>A, NM_001105568.4:c.53G>A, NM_001105568.3:c.53G>A, NM_001105568.2:c.53G>A, NM_001105566.3:c.53G>A, NM_001105566.2:c.53G>A, NM_001105567.3:c.53G>A, NM_001105567.2:c.53G>A, NM_001243423.2:c.53G>A, NM_001243423.1:c.53G>A, NP_071396.4:p.Arg18Gln, NP_001099038.1:p.Arg18Gln, NP_001099036.1:p.Arg18Gln, NP_001099037.1:p.Arg18Gln, NP_001230352.1:p.Arg18Gln

Select item 131529912819.

rs1315299128 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:17951415 (GRCh38)
6:17951646 (GRCh37)
Canonical SPDI:: NC_000006.12:17951414:G:A
Gene:: KIF13A (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.17951415G>A, NC_000006.11:g.17951646G>A, NG_029766.1:g.41209C>T, NM_001243423.2:c.161C>T, NM_001243423.1:c.161C>T, NP_001230352.1:p.Ala54Val

Select item 129811918320.

rs1298119183 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:17951429 (GRCh38)
6:17951660 (GRCh37)
Canonical SPDI:: NC_000006.12:17951428:C:A
Gene:: KIF13A (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
HGVS:: NC_000006.12:g.17951429C>A, NC_000006.11:g.17951660C>A, NG_029766.1:g.41195G>T, NM_001243423.2:c.147G>T, NM_001243423.1:c.147G>T, NP_001230352.1:p.Arg49Ser

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