SNP Links for Protein (Select 37187860) - SNP

Links from Protein

Items: 1 to 20 of 287

<< First< Prev

Page of 15

Next >Last >>

Select item 14878600591.

rs1487860059 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:167137169 (GRCh38)
6:167550657 (GRCh37)
Canonical SPDI:: NC_000006.12:167137168:T:C
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.167137169T>C, NC_000006.11:g.167550657T>C, NM_004367.6:c.939T>C, NM_004367.5:c.939T>C, NM_031409.4:c.939T>C, NM_031409.3:c.939T>C, NM_001394582.1:c.939T>C

Select item 14845919912.

rs1484591991 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:167136306 (GRCh38)
6:167549794 (GRCh37)
Canonical SPDI:: NC_000006.12:167136305:T:C
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.00003/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (GnomAD_exomes)
C=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.167136306T>C, NC_000006.11:g.167549794T>C, NM_004367.6:c.76T>C, NM_004367.5:c.76T>C, NM_031409.4:c.76T>C, NM_031409.3:c.76T>C, NM_001394582.1:c.76T>C, NP_004358.2:p.Tyr26His, NP_113597.2:p.Tyr26His, NP_001381511.1:p.Tyr26His

Select item 14758374393.

rs1475837439 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:167136653 (GRCh38)
6:167550141 (GRCh37)
Canonical SPDI:: NC_000006.12:167136652:G:T
Gene:: CCR6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.167136653G>T, NC_000006.11:g.167550141G>T, NM_004367.6:c.423G>T, NM_004367.5:c.423G>T, NM_031409.4:c.423G>T, NM_031409.3:c.423G>T, NM_001394582.1:c.423G>T, NP_004358.2:p.Met141Ile, NP_113597.2:p.Met141Ile, NP_001381511.1:p.Met141Ile

Select item 14726604044.

rs1472660404 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:167136445 (GRCh38)
6:167549933 (GRCh37)
Canonical SPDI:: NC_000006.12:167136444:C:A
Gene:: CCR6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.167136445C>A, NC_000006.11:g.167549933C>A, NM_004367.6:c.215C>A, NM_004367.5:c.215C>A, NM_031409.4:c.215C>A, NM_031409.3:c.215C>A, NM_001394582.1:c.215C>A, NP_004358.2:p.Ala72Asp, NP_113597.2:p.Ala72Asp, NP_001381511.1:p.Ala72Asp

Select item 14695272275.

rs1469527227 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:167136959 (GRCh38)
6:167550447 (GRCh37)
Canonical SPDI:: NC_000006.12:167136958:A:G
Gene:: CCR6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.167136959A>G, NC_000006.11:g.167550447A>G, NM_004367.6:c.729A>G, NM_004367.5:c.729A>G, NM_031409.4:c.729A>G, NM_031409.3:c.729A>G, NM_001394582.1:c.729A>G

Select item 14556277636.

rs1455627763 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:167136556 (GRCh38)
6:167550044 (GRCh37)
Canonical SPDI:: NC_000006.12:167136555:G:A
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000043/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.167136556G>A, NC_000006.11:g.167550044G>A, NM_004367.6:c.326G>A, NM_004367.5:c.326G>A, NM_031409.4:c.326G>A, NM_031409.3:c.326G>A, NM_001394582.1:c.326G>A, NP_004358.2:p.Gly109Asp, NP_113597.2:p.Gly109Asp, NP_001381511.1:p.Gly109Asp

Select item 14468419127.

rs1446841912 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:167136902 (GRCh38)
6:167550390 (GRCh37)
Canonical SPDI:: NC_000006.12:167136901:T:C
Gene:: CCR6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000006.12:g.167136902T>C, NC_000006.11:g.167550390T>C, NM_004367.6:c.672T>C, NM_004367.5:c.672T>C, NM_031409.4:c.672T>C, NM_031409.3:c.672T>C, NM_001394582.1:c.672T>C

Select item 14426506468.

rs1442650646 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 6:167136478 (GRCh38)
6:167549966 (GRCh37)
Canonical SPDI:: NC_000006.12:167136477:T:A,NC_000006.12:167136477:T:C
Gene:: CCR6 (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)
HGVS:: NC_000006.12:g.167136478T>A, NC_000006.12:g.167136478T>C, NC_000006.11:g.167549966T>A, NC_000006.11:g.167549966T>C, NM_004367.6:c.248T>A, NM_004367.6:c.248T>C, NM_004367.5:c.248T>A, NM_004367.5:c.248T>C, NM_031409.4:c.248T>A, NM_031409.4:c.248T>C, NM_031409.3:c.248T>A, NM_031409.3:c.248T>C, NM_001394582.1:c.248T>A, NM_001394582.1:c.248T>C, NP_004358.2:p.Val83Asp, NP_004358.2:p.Val83Ala, NP_113597.2:p.Val83Asp, NP_113597.2:p.Val83Ala, NP_001381511.1:p.Val83Asp, NP_001381511.1:p.Val83Ala

Select item 14418500259.

rs1441850025 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:167136840 (GRCh38)
6:167550328 (GRCh37)
Canonical SPDI:: NC_000006.12:167136839:G:A
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.167136840G>A, NC_000006.11:g.167550328G>A, NM_004367.6:c.610G>A, NM_004367.5:c.610G>A, NM_031409.4:c.610G>A, NM_031409.3:c.610G>A, NM_001394582.1:c.610G>A, NP_004358.2:p.Val204Ile, NP_113597.2:p.Val204Ile, NP_001381511.1:p.Val204Ile

Select item 143863721610.

rs1438637216 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:167136675 (GRCh38)
6:167550163 (GRCh37)
Canonical SPDI:: NC_000006.12:167136674:C:T
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
HGVS:: NC_000006.12:g.167136675C>T, NC_000006.11:g.167550163C>T, NM_004367.6:c.445C>T, NM_004367.5:c.445C>T, NM_031409.4:c.445C>T, NM_031409.3:c.445C>T, NM_001394582.1:c.445C>T, NP_004358.2:p.Gln149Ter, NP_113597.2:p.Gln149Ter, NP_001381511.1:p.Gln149Ter

Select item 143294231611.

rs1432942316 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:167136813 (GRCh38)
6:167550301 (GRCh37)
Canonical SPDI:: NC_000006.12:167136812:G:A
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.167136813G>A, NC_000006.11:g.167550301G>A, NM_004367.6:c.583G>A, NM_004367.5:c.583G>A, NM_031409.4:c.583G>A, NM_031409.3:c.583G>A, NM_001394582.1:c.583G>A, NP_004358.2:p.Asp195Asn, NP_113597.2:p.Asp195Asn, NP_001381511.1:p.Asp195Asn

Select item 142075329912.

rs1420753299 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 6:167136941 (GRCh38)
6:167550429 (GRCh37)
Canonical SPDI:: NC_000006.12:167136940:T:A,NC_000006.12:167136940:T:C
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.167136941T>A, NC_000006.12:g.167136941T>C, NC_000006.11:g.167550429T>A, NC_000006.11:g.167550429T>C, NM_004367.6:c.711T>A, NM_004367.6:c.711T>C, NM_004367.5:c.711T>A, NM_004367.5:c.711T>C, NM_031409.4:c.711T>A, NM_031409.4:c.711T>C, NM_031409.3:c.711T>A, NM_031409.3:c.711T>C, NM_001394582.1:c.711T>A, NM_001394582.1:c.711T>C

Select item 142011666613.

rs1420116666 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:167136883 (GRCh38)
6:167550371 (GRCh37)
Canonical SPDI:: NC_000006.12:167136882:A:G
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.167136883A>G, NC_000006.11:g.167550371A>G, NM_004367.6:c.653A>G, NM_004367.5:c.653A>G, NM_031409.4:c.653A>G, NM_031409.3:c.653A>G, NM_001394582.1:c.653A>G, NP_004358.2:p.Glu218Gly, NP_113597.2:p.Glu218Gly, NP_001381511.1:p.Glu218Gly

Select item 141079175414.

rs1410791754 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:167136451 (GRCh38)
6:167549939 (GRCh37)
Canonical SPDI:: NC_000006.12:167136450:A:G
Gene:: CCR6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.167136451A>G, NC_000006.11:g.167549939A>G, NM_004367.6:c.221A>G, NM_004367.5:c.221A>G, NM_031409.4:c.221A>G, NM_031409.3:c.221A>G, NM_001394582.1:c.221A>G, NP_004358.2:p.Tyr74Cys, NP_113597.2:p.Tyr74Cys, NP_001381511.1:p.Tyr74Cys

Select item 140979427115.

rs1409794271 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 6:167137312 (GRCh38)
6:167550800 (GRCh37)
Canonical SPDI:: NC_000006.12:167137311:G:A,NC_000006.12:167137311:G:C
Gene:: CCR6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.167137312G>A, NC_000006.12:g.167137312G>C, NC_000006.11:g.167550800G>A, NC_000006.11:g.167550800G>C, NM_004367.6:c.1082G>A, NM_004367.6:c.1082G>C, NM_004367.5:c.1082G>A, NM_004367.5:c.1082G>C, NM_031409.4:c.1082G>A, NM_031409.4:c.1082G>C, NM_031409.3:c.1082G>A, NM_031409.3:c.1082G>C, NM_001394582.1:c.1082G>A, NM_001394582.1:c.1082G>C, NP_004358.2:p.Ser361Asn, NP_004358.2:p.Ser361Thr, NP_113597.2:p.Ser361Asn, NP_113597.2:p.Ser361Thr, NP_001381511.1:p.Ser361Asn, NP_001381511.1:p.Ser361Thr

Select item 140782572516.

rs1407825725 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:167137247 (GRCh38)
6:167550735 (GRCh37)
Canonical SPDI:: NC_000006.12:167137246:G:A
Gene:: CCR6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.167137247G>A, NC_000006.11:g.167550735G>A, NM_004367.6:c.1017G>A, NM_004367.5:c.1017G>A, NM_031409.4:c.1017G>A, NM_031409.3:c.1017G>A, NM_001394582.1:c.1017G>A

Select item 140527761017.

rs1405277610 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:167137355 (GRCh38)
6:167550843 (GRCh37)
Canonical SPDI:: NC_000006.12:167137354:A:T
Gene:: CCR6 (Varview)
Functional Consequence:: stop_lost,terminator_codon_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.167137355A>T, NC_000006.11:g.167550843A>T, NM_004367.6:c.1125A>T, NM_004367.5:c.1125A>T, NM_031409.4:c.1125A>T, NM_031409.3:c.1125A>T, NM_001394582.1:c.1125A>T, NP_004358.2:p.Ter375Cys, NP_113597.2:p.Ter375Cys, NP_001381511.1:p.Ter375Cys

Select item 140461324618.

rs1404613246 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:167136872 (GRCh38)
6:167550360 (GRCh37)
Canonical SPDI:: NC_000006.12:167136871:G:A
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.167136872G>A, NC_000006.11:g.167550360G>A, NM_004367.6:c.642G>A, NM_004367.5:c.642G>A, NM_031409.4:c.642G>A, NM_031409.3:c.642G>A, NM_001394582.1:c.642G>A, NP_004358.2:p.Met214Ile, NP_113597.2:p.Met214Ile, NP_001381511.1:p.Met214Ile

Select item 140152458719.

rs1401524587 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:167136576 (GRCh38)
6:167550064 (GRCh37)
Canonical SPDI:: NC_000006.12:167136575:G:A,NC_000006.12:167136575:G:T
Gene:: CCR6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.167136576G>A, NC_000006.12:g.167136576G>T, NC_000006.11:g.167550064G>A, NC_000006.11:g.167550064G>T, NM_004367.6:c.346G>A, NM_004367.6:c.346G>T, NM_004367.5:c.346G>A, NM_004367.5:c.346G>T, NM_031409.4:c.346G>A, NM_031409.4:c.346G>T, NM_031409.3:c.346G>A, NM_031409.3:c.346G>T, NM_001394582.1:c.346G>A, NM_001394582.1:c.346G>T, NP_004358.2:p.Ala116Thr, NP_004358.2:p.Ala116Ser, NP_113597.2:p.Ala116Thr, NP_113597.2:p.Ala116Ser, NP_001381511.1:p.Ala116Thr, NP_001381511.1:p.Ala116Ser

Select item 139903753320.

rs1399037533 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:167136362 (GRCh38)
6:167549850 (GRCh37)
Canonical SPDI:: NC_000006.12:167136361:C:A
Gene:: CCR6 (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.167136362C>A, NC_000006.11:g.167549850C>A, NM_004367.6:c.132C>A, NM_004367.5:c.132C>A, NM_031409.4:c.132C>A, NM_031409.3:c.132C>A, NM_001394582.1:c.132C>A, NP_004358.2:p.Phe44Leu, NP_113597.2:p.Phe44Leu, NP_001381511.1:p.Phe44Leu

<< First< Prev

Page of 15

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 287

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity