SNP Links for Gene (Select 6358) - SNP

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Select item 14908489971.

rs1490848997 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:35986104 (GRCh38)
17:34313140 (GRCh37)
Canonical SPDI:: NC_000017.11:35986103:G:A
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.35986104G>A, NT_187614.1:g.220668G>A, NC_000017.10:g.34313140G>A

Select item 14903418842.

rs1490341884 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:35984185 (GRCh38)
17:34311221 (GRCh37)
Canonical SPDI:: NC_000017.11:35984184:A:C
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.35984185A>C, NT_187614.1:g.218749A>C, NC_000017.10:g.34311221A>C

Select item 14891522393.

rs1489152239 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:35984414 (GRCh38)
17:34311450 (GRCh37)
Canonical SPDI:: NC_000017.11:35984413:T:C
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_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_000017.11:g.35984414T>C, NT_187614.1:g.218978T>C, NC_000017.10:g.34311450T>C, NM_032962.5:c.166A>G, NM_032962.4:c.166A>G, NM_032963.4:c.118A>G, NM_032963.3:c.118A>G, NM_004167.4:c.*267A>G, NM_004166.4:c.118A>G, NR_027921.3:n.1155A>G, NR_027921.2:n.1162A>G, NR_027922.3:n.1107A>G, NR_027922.2:n.1114A>G, NM_004167.3:c.*267A>G, NM_004166.3:c.118A>G, NM_032964.3:c.*219A>G, NM_004167.2:c.*267A>G, NM_032964.2:c.*219A>G, NM_004166.2:c.118A>G, NM_032964.1:c.*219A>G, NM_004167.1:c.*267A>G, NM_004166.1:c.118A>G, NP_116738.1:p.Thr56Ala, NP_116739.1:p.Thr40Ala

Select item 14883093034.

rs1488309303 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:35984691 (GRCh38)
17:34311727 (GRCh37)
Canonical SPDI:: NC_000017.11:35984690:G:C
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.35984691G>C, NT_187614.1:g.219255G>C, NC_000017.10:g.34311727G>C

Select item 14882036265.

rs1488203626 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:35984506 (GRCh38)
17:34311542 (GRCh37)
Canonical SPDI:: NC_000017.11:35984505:A:G
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.35984506A>G, NT_187614.1:g.219070A>G, NC_000017.10:g.34311542A>G

Select item 14876038726.

rs1487603872 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:35984153 (GRCh38)
17:34311189 (GRCh37)
Canonical SPDI:: NC_000017.11:35984152:G:T
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.35984153G>T, NT_187614.1:g.218717G>T, NC_000017.10:g.34311189G>T

Select item 14870267677.

rs1487026767 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGAAG>- [Show Flanks]
Chromosome:: 17:35986780 (GRCh38)
17:34313816 (GRCh37)
Canonical SPDI:: NC_000017.11:35986774:GGAAGGGAAG:GGAAG
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGAAGGGAAG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.35986775GGAAG[1], NT_187614.1:g.221339GGAAG[1], NC_000017.10:g.34313811GGAAG[1]

Select item 14860132948.

rs1486013294 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 17:35985637 (GRCh38)
17:34312673 (GRCh37)
Canonical SPDI:: NC_000017.11:35985636:C:A
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.35985637C>A, NT_187614.1:g.220201C>A, NC_000017.10:g.34312673C>A

Select item 14859988949.

rs1485998894 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 17:35987954 (GRCh38)
17:34314990 (GRCh37)
Canonical SPDI:: NC_000017.11:35987953:A:G,NC_000017.11:35987953:A:T
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000017.11:g.35987954A>G, NC_000017.11:g.35987954A>T, NT_187614.1:g.222518A>G, NT_187614.1:g.222518A>T, NC_000017.10:g.34314990A>G, NC_000017.10:g.34314990A>T

Select item 148563887310.

rs1485638873 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 17:35983187 (GRCh38)
17:34310223 (GRCh37)
Canonical SPDI:: NC_000017.11:35983186:C:
Gene:: CCL14 (Varview), CCL16 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: downstream_transcript_variant,2KB_upstream_variant,500B_downstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.35983187del, NT_187614.1:g.217751del, NC_000017.10:g.34310223del

Select item 148548476711.

rs1485484767 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35983532 (GRCh38)
17:34310568 (GRCh37)
Canonical SPDI:: NC_000017.11:35983531:C:T
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.35983532C>T, NT_187614.1:g.218096C>T, NC_000017.10:g.34310568C>T, NM_032962.5:c.*269G>A, NM_032963.4:c.*269G>A

Select item 148487569512.

rs1484875695 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35984428 (GRCh38)
17:34311464 (GRCh37)
Canonical SPDI:: NC_000017.11:35984427:C:T
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
HGVS:: NC_000017.11:g.35984428C>T, NT_187614.1:g.218992C>T, NC_000017.10:g.34311464C>T, NM_032962.5:c.152G>A, NM_032962.4:c.152G>A, NM_032963.4:c.104G>A, NM_032963.3:c.104G>A, NM_004167.4:c.*253G>A, NM_004166.4:c.104G>A, NR_027921.3:n.1141G>A, NR_027921.2:n.1148G>A, NR_027922.3:n.1093G>A, NR_027922.2:n.1100G>A, NM_004167.3:c.*253G>A, NM_004166.3:c.104G>A, NM_032964.3:c.*205G>A, NM_032964.2:c.*205G>A, NM_004166.2:c.104G>A, NM_004167.2:c.*253G>A, NM_032964.1:c.*205G>A, NM_004167.1:c.*253G>A, NM_004166.1:c.104G>A, NP_116738.1:p.Cys51Tyr, NP_116739.1:p.Cys35Tyr

Select item 148440310913.

rs1484403109 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:35986401 (GRCh38)
17:34313437 (GRCh37)
Canonical SPDI:: NC_000017.11:35986400:G:C
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.35986401G>C, NT_187614.1:g.220965G>C, NC_000017.10:g.34313437G>C

Select item 148368379514.

rs1483683795 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35984362 (GRCh38)
17:34311398 (GRCh37)
Canonical SPDI:: NC_000017.11:35984361:C:T
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.35984362C>T, NT_187614.1:g.218926C>T, NC_000017.10:g.34311398C>T, NM_032962.5:c.218G>A, NM_032962.4:c.218G>A, NM_032963.4:c.170G>A, NM_032963.3:c.170G>A, NM_004167.4:c.*319G>A, NM_004166.4:c.170G>A, NR_027921.3:n.1207G>A, NR_027921.2:n.1214G>A, NR_027922.3:n.1159G>A, NR_027922.2:n.1166G>A, NM_004167.3:c.*319G>A, NM_004166.3:c.170G>A, NM_032964.3:c.*271G>A, NM_032964.2:c.*271G>A, NM_004166.2:c.170G>A, NM_004167.2:c.*319G>A, NM_032964.1:c.*271G>A, NM_004167.1:c.*319G>A, NM_004166.1:c.170G>A, NP_116738.1:p.Ser73Asn, NP_116739.1:p.Ser57Asn

Select item 148359194115.

rs1483591941 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:35983299 (GRCh38)
17:34310335 (GRCh37)
Canonical SPDI:: NC_000017.11:35983298:T:C
Gene:: CCL14 (Varview), CCL16 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: downstream_transcript_variant,2KB_upstream_variant,500B_downstream_variant,3_prime_UTR_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.35983299T>C, NT_187614.1:g.217863T>C, NC_000017.10:g.34310335T>C, NM_032962.5:c.*502A>G, NM_032963.4:c.*502A>G

Select item 148354020916.

rs1483540209 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:35988095 (GRCh38)
17:34315131 (GRCh37)
Canonical SPDI:: NC_000017.11:35988094:A:G
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.35988095A>G, NT_187614.1:g.222659A>G, NC_000017.10:g.34315131A>G

Select item 148248495717.

rs1482484957 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 17:35987282 (GRCh38)
17:34314318 (GRCh37)
Canonical SPDI:: NC_000017.11:35987281:C:A,NC_000017.11:35987281:C:G
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.35987282C>A, NC_000017.11:g.35987282C>G, NT_187614.1:g.221846C>A, NT_187614.1:g.221846C>G, NC_000017.10:g.34314318C>A, NC_000017.10:g.34314318C>G

Select item 148159860518.

rs1481598605 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCCT>- [Show Flanks]
Chromosome:: 17:35986526 (GRCh38)
17:34313562 (GRCh37)
Canonical SPDI:: NC_000017.11:35986524:TCCCT:T
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.35986526_35986529del, NT_187614.1:g.221090_221093del, NC_000017.10:g.34313562_34313565del

Select item 148063766719.

rs1480637667 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:35986776 (GRCh38)
17:34313812 (GRCh37)
Canonical SPDI:: NC_000017.11:35986775:G:T
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000026/7 (TOPMED)
HGVS:: NC_000017.11:g.35986776G>T, NT_187614.1:g.221340G>T, NC_000017.10:g.34313812G>T

Select item 148035101820.

rs1480351018 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:35987976 (GRCh38)
17:34315012 (GRCh37)
Canonical SPDI:: NC_000017.11:35987975:T:C
Gene:: CCL14 (Varview), CCL15-CCL14 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.35987976T>C, NT_187614.1:g.222540T>C, NC_000017.10:g.34315012T>C

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