SNP Links for Protein (Select 807066366) - SNP

Links from Protein

Items: 1 to 20 of 416

<< First< Prev

Page of 21

Next >Last >>

Select item 14871882101.

rs1487188210 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 5:10261574 (GRCh38)
5:10261686 (GRCh37)
Canonical SPDI:: NC_000005.10:10261573:A:C
Gene:: CCT5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000005.10:g.10261574A>C, NC_000005.9:g.10261686A>C, NG_012160.1:g.16405A>C, NM_012073.5:c.1008A>C, NM_012073.4:c.1008A>C, NM_012073.3:c.1008A>C, NM_001306156.2:c.894A>C, NM_001306156.1:c.894A>C, NM_001306155.2:c.729A>C, NM_001306155.1:c.729A>C, NM_001306154.2:c.843A>C, NM_001306154.1:c.843A>C, NM_001306153.1:c.945A>C

Select item 14818354202.

rs1481835420 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:10258150 (GRCh38)
5:10258262 (GRCh37)
Canonical SPDI:: NC_000005.10:10258149:G:C
Gene:: CCT5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000049/13 (TOPMED)
C=0.00005/7 (GnomAD)
HGVS:: NC_000005.10:g.10258150G>C, NC_000005.9:g.10258262G>C, NG_012160.1:g.12981G>C, NM_012073.5:c.570G>C, NM_012073.4:c.570G>C, NM_012073.3:c.570G>C, NM_001306156.2:c.456G>C, NM_001306156.1:c.456G>C, NM_001306155.2:c.291G>C, NM_001306155.1:c.291G>C, NM_001306154.2:c.405G>C, NM_001306154.1:c.405G>C, NM_001306153.1:c.507G>C

Select item 14793520263.

rs1479352026 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 5:10255979 (GRCh38)
5:10256091 (GRCh37)
Canonical SPDI:: NC_000005.10:10255978:A:C,NC_000005.10:10255978:A:T
Gene:: CCT5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000051/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10255979A>C, NC_000005.10:g.10255979A>T, NC_000005.9:g.10256091A>C, NC_000005.9:g.10256091A>T, NG_012160.1:g.10810A>C, NG_012160.1:g.10810A>T, NM_012073.5:c.356A>C, NM_012073.5:c.356A>T, NM_012073.4:c.356A>C, NM_012073.4:c.356A>T, NM_012073.3:c.356A>C, NM_012073.3:c.356A>T, NM_001306156.2:c.242A>C, NM_001306156.2:c.242A>T, NM_001306156.1:c.242A>C, NM_001306156.1:c.242A>T, NM_001306155.2:c.77A>C, NM_001306155.2:c.77A>T, NM_001306155.1:c.77A>C, NM_001306155.1:c.77A>T, NM_001306154.2:c.191A>C, NM_001306154.2:c.191A>T, NM_001306154.1:c.191A>C, NM_001306154.1:c.191A>T, NM_001306153.1:c.293A>C, NM_001306153.1:c.293A>T, NP_036205.1:p.Glu119Ala, NP_036205.1:p.Glu119Val, NP_001293085.1:p.Glu81Ala, NP_001293085.1:p.Glu81Val, NP_001293084.1:p.Glu26Ala, NP_001293084.1:p.Glu26Val, NP_001293083.1:p.Glu64Ala, NP_001293083.1:p.Glu64Val, NP_001293082.1:p.Glu98Ala, NP_001293082.1:p.Glu98Val

Select item 14775901014.

rs1477590101 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:10261711 (GRCh38)
5:10261823 (GRCh37)
Canonical SPDI:: NC_000005.10:10261710:C:T
Gene:: CCT5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.10261711C>T, NC_000005.9:g.10261823C>T, NG_012160.1:g.16542C>T, NM_012073.5:c.1145C>T, NM_012073.4:c.1145C>T, NM_012073.3:c.1145C>T, NM_001306156.2:c.1031C>T, NM_001306156.1:c.1031C>T, NM_001306155.2:c.866C>T, NM_001306155.1:c.866C>T, NM_001306154.2:c.980C>T, NM_001306154.1:c.980C>T, NM_001306153.1:c.1082C>T, NP_036205.1:p.Ala382Val, NP_001293085.1:p.Ala344Val, NP_001293084.1:p.Ala289Val, NP_001293083.1:p.Ala327Val, NP_001293082.1:p.Ala361Val

Select item 14747614505.

rs1474761450 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:10256144 (GRCh38)
5:10256256 (GRCh37)
Canonical SPDI:: NC_000005.10:10256143:G:A
Gene:: CCT5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.10256144G>A, NC_000005.9:g.10256256G>A, NG_012160.1:g.10975G>A, NM_012073.5:c.521G>A, NM_012073.4:c.521G>A, NM_012073.3:c.521G>A, NM_001306156.2:c.407G>A, NM_001306156.1:c.407G>A, NM_001306155.2:c.242G>A, NM_001306155.1:c.242G>A, NM_001306154.2:c.356G>A, NM_001306154.1:c.356G>A, NM_001306153.1:c.458G>A, NP_036205.1:p.Gly174Asp, NP_001293085.1:p.Gly136Asp, NP_001293084.1:p.Gly81Asp, NP_001293083.1:p.Gly119Asp, NP_001293082.1:p.Gly153Asp

Select item 14732086926.

rs1473208692 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:10255984 (GRCh38)
5:10256096 (GRCh37)
Canonical SPDI:: NC_000005.10:10255983:G:A
Gene:: CCT5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.10255984G>A, NC_000005.9:g.10256096G>A, NG_012160.1:g.10815G>A, NM_012073.5:c.361G>A, NM_012073.4:c.361G>A, NM_012073.3:c.361G>A, NM_001306156.2:c.247G>A, NM_001306156.1:c.247G>A, NM_001306155.2:c.82G>A, NM_001306155.1:c.82G>A, NM_001306154.2:c.196G>A, NM_001306154.1:c.196G>A, NM_001306153.1:c.298G>A, NP_036205.1:p.Glu121Lys, NP_001293085.1:p.Glu83Lys, NP_001293084.1:p.Glu28Lys, NP_001293083.1:p.Glu66Lys, NP_001293082.1:p.Glu100Lys

Select item 14719197277.

rs1471919727 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:10254183 (GRCh38)
5:10254295 (GRCh37)
Canonical SPDI:: NC_000005.10:10254182:G:T
Gene:: CCT5 (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_000005.10:g.10254183G>T, NC_000005.9:g.10254295G>T, NG_012160.1:g.9014G>T, NM_012073.5:c.144G>T, NM_012073.4:c.144G>T, NM_012073.3:c.144G>T, NM_001306156.2:c.30G>T, NM_001306156.1:c.30G>T, NM_001306155.2:c.30G>T, NM_001306155.1:c.30G>T, NM_001306154.2:c.144G>T, NM_001306154.1:c.144G>T, NM_001306153.1:c.81G>T, NP_036205.1:p.Met48Ile, NP_001293085.1:p.Met10Ile, NP_001293084.1:p.Met10Ile, NP_001293083.1:p.Met48Ile, NP_001293082.1:p.Met27Ile

Select item 14711217628.

rs1471121762 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 5:10258126 (GRCh38)
5:10258238 (GRCh37)
Canonical SPDI:: NC_000005.10:10258125:C:A
Gene:: CCT5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.10258126C>A, NC_000005.9:g.10258238C>A, NG_012160.1:g.12957C>A, NM_012073.5:c.546C>A, NM_012073.4:c.546C>A, NM_012073.3:c.546C>A, NM_001306156.2:c.432C>A, NM_001306156.1:c.432C>A, NM_001306155.2:c.267C>A, NM_001306155.1:c.267C>A, NM_001306154.2:c.381C>A, NM_001306154.1:c.381C>A, NM_001306153.1:c.483C>A, NP_036205.1:p.His182Gln, NP_001293085.1:p.His144Gln, NP_001293084.1:p.His89Gln, NP_001293083.1:p.His127Gln, NP_001293082.1:p.His161Gln

Select item 14662113409.

rs1466211340 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:10264694 (GRCh38)
5:10264806 (GRCh37)
Canonical SPDI:: NC_000005.10:10264693:A:G
Gene:: CCT5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000005.10:g.10264694A>G, NC_000005.9:g.10264806A>G, NG_012160.1:g.19525A>G, NM_012073.5:c.1537A>G, NM_012073.4:c.1537A>G, NM_012073.3:c.1537A>G, NM_001306156.2:c.1423A>G, NM_001306156.1:c.1423A>G, NM_001306155.2:c.1258A>G, NM_001306155.1:c.1258A>G, NM_001306154.2:c.1372A>G, NM_001306154.1:c.1372A>G, NM_001306153.1:c.1474A>G, NP_036205.1:p.Lys513Glu, NP_001293085.1:p.Lys475Glu, NP_001293084.1:p.Lys420Glu, NP_001293083.1:p.Lys458Glu, NP_001293082.1:p.Lys492Glu

Select item 146261293110.

rs1462612931 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:10258183 (GRCh38)
5:10258295 (GRCh37)
Canonical SPDI:: NC_000005.10:10258182:G:C
Gene:: CCT5 (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=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10258183G>C, NC_000005.9:g.10258295G>C, NG_012160.1:g.13014G>C, NM_012073.5:c.603G>C, NM_012073.4:c.603G>C, NM_012073.3:c.603G>C, NM_001306156.2:c.489G>C, NM_001306156.1:c.489G>C, NM_001306155.2:c.324G>C, NM_001306155.1:c.324G>C, NM_001306154.2:c.438G>C, NM_001306154.1:c.438G>C, NM_001306153.1:c.540G>C

Select item 146232956811.

rs1462329568 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 5:10255968 (GRCh38)
5:10256080 (GRCh37)
Canonical SPDI:: NC_000005.10:10255967:C:G
Gene:: CCT5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000005.10:g.10255968C>G, NC_000005.9:g.10256080C>G, NG_012160.1:g.10799C>G, NM_012073.5:c.345C>G, NM_012073.4:c.345C>G, NM_012073.3:c.345C>G, NM_001306156.2:c.231C>G, NM_001306156.1:c.231C>G, NM_001306155.2:c.66C>G, NM_001306155.1:c.66C>G, NM_001306154.2:c.180C>G, NM_001306154.1:c.180C>G, NM_001306153.1:c.282C>G

Select item 146117429812.

rs1461174298 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 5:10258270 (GRCh38)
5:10258382 (GRCh37)
Canonical SPDI:: NC_000005.10:10258269:G:A,NC_000005.10:10258269:G:C
Gene:: CCT5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10258270G>A, NC_000005.10:g.10258270G>C, NC_000005.9:g.10258382G>A, NC_000005.9:g.10258382G>C, NG_012160.1:g.13101G>A, NG_012160.1:g.13101G>C, NM_012073.5:c.690G>A, NM_012073.5:c.690G>C, NM_012073.4:c.690G>A, NM_012073.4:c.690G>C, NM_012073.3:c.690G>A, NM_012073.3:c.690G>C, NM_001306156.2:c.576G>A, NM_001306156.2:c.576G>C, NM_001306156.1:c.576G>A, NM_001306156.1:c.576G>C, NM_001306155.2:c.411G>A, NM_001306155.2:c.411G>C, NM_001306155.1:c.411G>A, NM_001306155.1:c.411G>C, NM_001306154.2:c.525G>A, NM_001306154.2:c.525G>C, NM_001306154.1:c.525G>A, NM_001306154.1:c.525G>C, NM_001306153.1:c.627G>A, NM_001306153.1:c.627G>C

Select item 146089017413.

rs1460890174 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:10261589 (GRCh38)
5:10261701 (GRCh37)
Canonical SPDI:: NC_000005.10:10261588:C:T
Gene:: CCT5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.10261589C>T, NC_000005.9:g.10261701C>T, NG_012160.1:g.16420C>T, NM_012073.5:c.1023C>T, NM_012073.4:c.1023C>T, NM_012073.3:c.1023C>T, NM_001306156.2:c.909C>T, NM_001306156.1:c.909C>T, NM_001306155.2:c.744C>T, NM_001306155.1:c.744C>T, NM_001306154.2:c.858C>T, NM_001306154.1:c.858C>T, NM_001306153.1:c.960C>T

Select item 145658175014.

rs1456581750 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:10262547 (GRCh38)
5:10262659 (GRCh37)
Canonical SPDI:: NC_000005.10:10262546:A:G
Gene:: CCT5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10262547A>G, NC_000005.9:g.10262659A>G, NG_012160.1:g.17378A>G, NM_012073.5:c.1246A>G, NM_012073.4:c.1246A>G, NM_012073.3:c.1246A>G, NM_001306156.2:c.1132A>G, NM_001306156.1:c.1132A>G, NM_001306155.2:c.967A>G, NM_001306155.1:c.967A>G, NM_001306154.2:c.1081A>G, NM_001306154.1:c.1081A>G, NM_001306153.1:c.1183A>G, NP_036205.1:p.Asn416Asp, NP_001293085.1:p.Asn378Asp, NP_001293084.1:p.Asn323Asp, NP_001293083.1:p.Asn361Asp, NP_001293082.1:p.Asn395Asp

Select item 145489642715.

rs1454896427 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 5:10258233 (GRCh38)
5:10258345 (GRCh37)
Canonical SPDI:: NC_000005.10:10258232:G:C
Gene:: CCT5 (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=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.10258233G>C, NC_000005.9:g.10258345G>C, NG_012160.1:g.13064G>C, NM_012073.5:c.653G>C, NM_012073.4:c.653G>C, NM_012073.3:c.653G>C, NM_001306156.2:c.539G>C, NM_001306156.1:c.539G>C, NM_001306155.2:c.374G>C, NM_001306155.1:c.374G>C, NM_001306154.2:c.488G>C, NM_001306154.1:c.488G>C, NM_001306153.1:c.590G>C, NP_036205.1:p.Arg218Thr, NP_001293085.1:p.Arg180Thr, NP_001293084.1:p.Arg125Thr, NP_001293083.1:p.Arg163Thr, NP_001293082.1:p.Arg197Thr

Select item 145442873116.

rs1454428731 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:10258252 (GRCh38)
5:10258364 (GRCh37)
Canonical SPDI:: NC_000005.10:10258251:G:T
Gene:: CCT5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.10258252G>T, NC_000005.9:g.10258364G>T, NG_012160.1:g.13083G>T, NM_012073.5:c.672G>T, NM_012073.4:c.672G>T, NM_012073.3:c.672G>T, NM_001306156.2:c.558G>T, NM_001306156.1:c.558G>T, NM_001306155.2:c.393G>T, NM_001306155.1:c.393G>T, NM_001306154.2:c.507G>T, NM_001306154.1:c.507G>T, NM_001306153.1:c.609G>T

Select item 144417804117.

rs1444178041 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:10258166 (GRCh38)
5:10258278 (GRCh37)
Canonical SPDI:: NC_000005.10:10258165:G:A
Gene:: CCT5 (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_000005.10:g.10258166G>A, NC_000005.9:g.10258278G>A, NG_012160.1:g.12997G>A, NM_012073.5:c.586G>A, NM_012073.4:c.586G>A, NM_012073.3:c.586G>A, NM_001306156.2:c.472G>A, NM_001306156.1:c.472G>A, NM_001306155.2:c.307G>A, NM_001306155.1:c.307G>A, NM_001306154.2:c.421G>A, NM_001306154.1:c.421G>A, NM_001306153.1:c.523G>A, NP_036205.1:p.Val196Ile, NP_001293085.1:p.Val158Ile, NP_001293084.1:p.Val103Ile, NP_001293083.1:p.Val141Ile, NP_001293082.1:p.Val175Ile

Select item 144005009918.

rs1440050099 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:10256014 (GRCh38)
5:10256126 (GRCh37)
Canonical SPDI:: NC_000005.10:10256013:A:G
Gene:: CCT5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000005.10:g.10256014A>G, NC_000005.9:g.10256126A>G, NG_012160.1:g.10845A>G, NM_012073.5:c.391A>G, NM_012073.4:c.391A>G, NM_012073.3:c.391A>G, NM_001306156.2:c.277A>G, NM_001306156.1:c.277A>G, NM_001306155.2:c.112A>G, NM_001306155.1:c.112A>G, NM_001306154.2:c.226A>G, NM_001306154.1:c.226A>G, NM_001306153.1:c.328A>G, NP_036205.1:p.Ile131Val, NP_001293085.1:p.Ile93Val, NP_001293084.1:p.Ile38Val, NP_001293083.1:p.Ile76Val, NP_001293082.1:p.Ile110Val

Select item 143809440319.

rs1438094403 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:10263222 (GRCh38)
5:10263334 (GRCh37)
Canonical SPDI:: NC_000005.10:10263221:A:G
Gene:: CCT5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.10263222A>G, NC_000005.9:g.10263334A>G, NG_012160.1:g.18053A>G, NM_012073.5:c.1406A>G, NM_012073.4:c.1406A>G, NM_012073.3:c.1406A>G, NM_001306156.2:c.1292A>G, NM_001306156.1:c.1292A>G, NM_001306155.2:c.1127A>G, NM_001306155.1:c.1127A>G, NM_001306154.2:c.1241A>G, NM_001306154.1:c.1241A>G, NM_001306153.1:c.1343A>G, NP_036205.1:p.Asn469Ser, NP_001293085.1:p.Asn431Ser, NP_001293084.1:p.Asn376Ser, NP_001293083.1:p.Asn414Ser, NP_001293082.1:p.Asn448Ser

Select item 142896127720.

rs1428961277 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:10254739 (GRCh38)
5:10254851 (GRCh37)
Canonical SPDI:: NC_000005.10:10254738:T:C
Gene:: CCT5 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.10254739T>C, NC_000005.9:g.10254851T>C, NG_012160.1:g.9570T>C, NM_012073.5:c.232T>C, NM_012073.4:c.232T>C, NM_012073.3:c.232T>C, NM_001306156.2:c.118T>C, NM_001306156.1:c.118T>C, NM_001306153.1:c.169T>C

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 416

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity