SNP Links for Protein (Select 45439355) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Protein

Items: 1 to 20 of 227

<< First< Prev

Page of 12

Next >Last >>

Select item 14885414701.

rs1488541470 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:54022072 (GRCh38)
8:54934632 (GRCh37)
Canonical SPDI:: NC_000008.11:54022071:C:T
Gene:: TCEA1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,genic_upstream_transcript_variant,5_prime_UTR_variant,coding_sequence_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.54022072C>T, NC_000008.10:g.54934632C>T, NM_006756.4:c.54G>A, NM_006756.3:c.54G>A, NM_006756.2:c.54G>A, NM_201437.3:c.54G>A, NM_201437.2:c.54G>A, NM_201437.1:c.54G>A, NR_109901.2:n.377G>A, NR_109901.1:n.385G>A, XM_006716467.2:c.-137G>A, XM_006716467.1:c.-137G>A, NR_109902.2:n.377G>A, NR_109902.1:n.385G>A

Select item 14784912922.

rs1478491292 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:53979118 (GRCh38)
8:54891678 (GRCh37)
Canonical SPDI:: NC_000008.11:53979117:G:A
Gene:: TCEA1 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53979118G>A, NC_000008.10:g.54891678G>A, NM_006756.4:c.732C>T, NM_006756.3:c.732C>T, NM_006756.2:c.732C>T, NM_201437.3:c.669C>T, NM_201437.2:c.669C>T, NM_201437.1:c.669C>T, NR_109901.2:n.1256C>T, NR_109901.1:n.1264C>T, XM_011517578.2:c.627C>T, XM_011517578.1:c.627C>T, XM_006716467.2:c.591C>T, XM_006716467.1:c.591C>T, NR_109902.2:n.503C>T, NR_109902.1:n.511C>T

Select item 14719329823.

rs1471932982 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:53984517 (GRCh38)
8:54897077 (GRCh37)
Canonical SPDI:: NC_000008.11:53984516:G:A
Gene:: TCEA1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000032/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53984517G>A, NC_000008.10:g.54897077G>A, NM_006756.4:c.524C>T, NM_006756.3:c.524C>T, NM_006756.2:c.524C>T, NM_201437.3:c.461C>T, NM_201437.2:c.461C>T, NM_201437.1:c.461C>T, NR_109901.2:n.1048C>T, NR_109901.1:n.1056C>T, XM_011517578.2:c.419C>T, XM_011517578.1:c.419C>T, XM_006716467.2:c.383C>T, XM_006716467.1:c.383C>T, NP_006747.1:p.Ala175Val, NP_958845.1:p.Ala154Val, XP_011515880.1:p.Ala140Val, XP_006716530.1:p.Ala128Val

Select item 14658971994.

rs1465897199 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:53986998 (GRCh38)
8:54899558 (GRCh37)
Canonical SPDI:: NC_000008.11:53986997:T:G
Gene:: TCEA1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant,intron_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_000008.11:g.53986998T>G, NC_000008.10:g.54899558T>G, NM_006756.4:c.494A>C, NM_006756.3:c.494A>C, NM_006756.2:c.494A>C, NM_201437.3:c.431A>C, NM_201437.2:c.431A>C, NM_201437.1:c.431A>C, NR_109901.2:n.1018A>C, NR_109901.1:n.1026A>C, XM_011517578.2:c.389A>C, XM_011517578.1:c.389A>C, XM_006716467.2:c.353A>C, XM_006716467.1:c.353A>C, NP_006747.1:p.Glu165Ala, NP_958845.1:p.Glu144Ala, XP_011515880.1:p.Glu130Ala, XP_006716530.1:p.Glu118Ala

Select item 14605556195.

rs1460555619 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53979125 (GRCh38)
8:54891685 (GRCh37)
Canonical SPDI:: NC_000008.11:53979124:T:C
Gene:: TCEA1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,missense_variant
HGVS:: NC_000008.11:g.53979125T>C, NC_000008.10:g.54891685T>C, NM_006756.4:c.725A>G, NM_006756.3:c.725A>G, NM_006756.2:c.725A>G, NM_201437.3:c.662A>G, NM_201437.2:c.662A>G, NM_201437.1:c.662A>G, NR_109901.2:n.1249A>G, NR_109901.1:n.1257A>G, XM_011517578.2:c.620A>G, XM_011517578.1:c.620A>G, XM_006716467.2:c.584A>G, XM_006716467.1:c.584A>G, NR_109902.2:n.496A>G, NR_109902.1:n.504A>G, NP_006747.1:p.Lys242Arg, NP_958845.1:p.Lys221Arg, XP_011515880.1:p.Lys207Arg, XP_006716530.1:p.Lys195Arg

Select item 14598634506.

rs1459863450 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 8:54022106 (GRCh38)
8:54934666 (GRCh37)
Canonical SPDI:: NC_000008.11:54022105:C:A,NC_000008.11:54022105:C:T
Gene:: TCEA1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
A=0.000177/3 (TOMMO)
HGVS:: NC_000008.11:g.54022106C>A, NC_000008.11:g.54022106C>T, NC_000008.10:g.54934666C>A, NC_000008.10:g.54934666C>T, NM_006756.4:c.20G>T, NM_006756.4:c.20G>A, NM_006756.3:c.20G>T, NM_006756.3:c.20G>A, NM_006756.2:c.20G>T, NM_006756.2:c.20G>A, NM_201437.3:c.20G>T, NM_201437.3:c.20G>A, NM_201437.2:c.20G>T, NM_201437.2:c.20G>A, NM_201437.1:c.20G>T, NM_201437.1:c.20G>A, NR_109901.2:n.343G>T, NR_109901.2:n.343G>A, NR_109901.1:n.351G>T, NR_109901.1:n.351G>A, XM_006716467.2:c.-171G>T, XM_006716467.2:c.-171G>A, XM_006716467.1:c.-171G>T, XM_006716467.1:c.-171G>A, NR_109902.2:n.343G>T, NR_109902.2:n.343G>A, NR_109902.1:n.351G>T, NR_109902.1:n.351G>A, NP_006747.1:p.Arg7Leu, NP_006747.1:p.Arg7His, NP_958845.1:p.Arg7Leu, NP_958845.1:p.Arg7His

Select item 14579977757.

rs1457997775 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:53988148 (GRCh38)
8:54900708 (GRCh37)
Canonical SPDI:: NC_000008.11:53988147:A:C
Gene:: TCEA1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53988148A>C, NC_000008.10:g.54900708A>C, NM_006756.4:c.432T>G, NM_006756.3:c.432T>G, NM_006756.2:c.432T>G, NM_201437.3:c.369T>G, NM_201437.2:c.369T>G, NM_201437.1:c.369T>G, NR_109901.2:n.956T>G, NR_109901.1:n.964T>G, XM_011517578.2:c.327T>G, XM_011517578.1:c.327T>G, XM_006716467.2:c.291T>G, XM_006716467.1:c.291T>G, NP_006747.1:p.Cys144Trp, NP_958845.1:p.Cys123Trp, XP_011515880.1:p.Cys109Trp, XP_006716530.1:p.Cys97Trp

Select item 14564969548.

rs1456496954 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53970398 (GRCh38)
8:54882958 (GRCh37)
Canonical SPDI:: NC_000008.11:53970397:T:C
Gene:: TCEA1 (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_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_000008.11:g.53970398T>C, NC_000008.10:g.54882958T>C, NM_006756.4:c.891A>G, NM_006756.3:c.891A>G, NM_006756.2:c.891A>G, NM_201437.3:c.828A>G, NM_201437.2:c.828A>G, NM_201437.1:c.828A>G, NR_109901.2:n.1590A>G, NR_109901.1:n.1598A>G, XM_011517578.2:c.786A>G, XM_011517578.1:c.786A>G, XM_006716467.2:c.750A>G, XM_006716467.1:c.750A>G, NR_109902.2:n.662A>G, NR_109902.1:n.670A>G

Select item 14548242009.

rs1454824200 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:54022086 (GRCh38)
8:54934646 (GRCh37)
Canonical SPDI:: NC_000008.11:54022085:T:G
Gene:: TCEA1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,missense_variant,genic_upstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000031/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.54022086T>G, NC_000008.10:g.54934646T>G, NM_006756.4:c.40A>C, NM_006756.3:c.40A>C, NM_006756.2:c.40A>C, NM_201437.3:c.40A>C, NM_201437.2:c.40A>C, NM_201437.1:c.40A>C, NR_109901.2:n.363A>C, NR_109901.1:n.371A>C, XM_006716467.2:c.-151A>C, XM_006716467.1:c.-151A>C, NR_109902.2:n.363A>C, NR_109902.1:n.371A>C, NP_006747.1:p.Lys14Gln, NP_958845.1:p.Lys14Gln

Select item 144634216210.

rs1446342162 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:53984405 (GRCh38)
8:54896965 (GRCh37)
Canonical SPDI:: NC_000008.11:53984404:A:C
Gene:: TCEA1 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant,non_coding_transcript_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_000008.11:g.53984405A>C, NC_000008.10:g.54896965A>C, NM_006756.4:c.636T>G, NM_006756.3:c.636T>G, NM_006756.2:c.636T>G, NM_201437.3:c.573T>G, NM_201437.2:c.573T>G, NM_201437.1:c.573T>G, NR_109901.2:n.1160T>G, NR_109901.1:n.1168T>G, XM_011517578.2:c.531T>G, XM_011517578.1:c.531T>G, XM_006716467.2:c.495T>G, XM_006716467.1:c.495T>G, NP_006747.1:p.Cys212Trp, NP_958845.1:p.Cys191Trp, XP_011515880.1:p.Cys177Trp, XP_006716530.1:p.Cys165Trp

Select item 144550373411.

rs1445503734 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:54022115 (GRCh38)
8:54934675 (GRCh37)
Canonical SPDI:: NC_000008.11:54022114:T:G
Gene:: TCEA1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,missense_variant,genic_upstream_transcript_variant,coding_sequence_variant,non_coding_transcript_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.54022115T>G, NC_000008.10:g.54934675T>G, NM_006756.4:c.11A>C, NM_006756.3:c.11A>C, NM_006756.2:c.11A>C, NM_201437.3:c.11A>C, NM_201437.2:c.11A>C, NM_201437.1:c.11A>C, NR_109901.2:n.334A>C, NR_109901.1:n.342A>C, XM_006716467.2:c.-180A>C, XM_006716467.1:c.-180A>C, NR_109902.2:n.334A>C, NR_109902.1:n.342A>C, NP_006747.1:p.Glu4Ala, NP_958845.1:p.Glu4Ala

Select item 144298985612.

rs1442989856 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 8:53988150 (GRCh38)
8:54900710 (GRCh37)
Canonical SPDI:: NC_000008.11:53988149:A:C
Gene:: TCEA1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.53988150A>C, NC_000008.10:g.54900710A>C, NM_006756.4:c.430T>G, NM_006756.3:c.430T>G, NM_006756.2:c.430T>G, NM_201437.3:c.367T>G, NM_201437.2:c.367T>G, NM_201437.1:c.367T>G, NR_109901.2:n.954T>G, NR_109901.1:n.962T>G, XM_011517578.2:c.325T>G, XM_011517578.1:c.325T>G, XM_006716467.2:c.289T>G, XM_006716467.1:c.289T>G, NP_006747.1:p.Cys144Gly, NP_958845.1:p.Cys123Gly, XP_011515880.1:p.Cys109Gly, XP_006716530.1:p.Cys97Gly

Select item 144131312913.

rs1441313129 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53984435 (GRCh38)
8:54896995 (GRCh37)
Canonical SPDI:: NC_000008.11:53984434:T:C
Gene:: TCEA1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.000111/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53984435T>C, NC_000008.10:g.54896995T>C, NM_006756.4:c.606A>G, NM_006756.3:c.606A>G, NM_006756.2:c.606A>G, NM_201437.3:c.543A>G, NM_201437.2:c.543A>G, NM_201437.1:c.543A>G, NR_109901.2:n.1130A>G, NR_109901.1:n.1138A>G, XM_011517578.2:c.501A>G, XM_011517578.1:c.501A>G, XM_006716467.2:c.465A>G, XM_006716467.1:c.465A>G

Select item 144089387814.

rs1440893878 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 8:54000003 (GRCh38)
8:54912563 (GRCh37)
Canonical SPDI:: NC_000008.11:54000002:T:A
Gene:: TCEA1 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.54000003T>A, NC_000008.10:g.54912563T>A, NM_006756.4:c.174A>T, NM_006756.3:c.174A>T, NM_006756.2:c.174A>T, NM_201437.3:c.111A>T, NM_201437.2:c.111A>T, NM_201437.1:c.111A>T, NR_109901.2:n.698A>T, NR_109901.1:n.706A>T, XM_011517578.2:c.69A>T, XM_011517578.1:c.69A>T, XM_006716467.2:c.33A>T, XM_006716467.1:c.33A>T

Select item 142522004115.

rs1425220041 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:53999946 (GRCh38)
8:54912506 (GRCh37)
Canonical SPDI:: NC_000008.11:53999945:T:G
Gene:: TCEA1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant,non_coding_transcript_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_000008.11:g.53999946T>G, NC_000008.10:g.54912506T>G, NM_006756.4:c.231A>C, NM_006756.3:c.231A>C, NM_006756.2:c.231A>C, NM_201437.3:c.168A>C, NM_201437.2:c.168A>C, NM_201437.1:c.168A>C, NR_109901.2:n.755A>C, NR_109901.1:n.763A>C, XM_011517578.2:c.126A>C, XM_011517578.1:c.126A>C, XM_006716467.2:c.90A>C, XM_006716467.1:c.90A>C, NP_006747.1:p.Leu77Phe, NP_958845.1:p.Leu56Phe, XP_011515880.1:p.Leu42Phe, XP_006716530.1:p.Leu30Phe

Select item 141637997316.

rs1416379973 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:53979151 (GRCh38)
8:54891711 (GRCh37)
Canonical SPDI:: NC_000008.11:53979150:C:T
Gene:: TCEA1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.53979151C>T, NC_000008.10:g.54891711C>T, NM_006756.4:c.699G>A, NM_006756.3:c.699G>A, NM_006756.2:c.699G>A, NM_201437.3:c.636G>A, NM_201437.2:c.636G>A, NM_201437.1:c.636G>A, NR_109901.2:n.1223G>A, NR_109901.1:n.1231G>A, XM_011517578.2:c.594G>A, XM_011517578.1:c.594G>A, XM_006716467.2:c.558G>A, XM_006716467.1:c.558G>A, NR_109902.2:n.470G>A, NR_109902.1:n.478G>A

Select item 141575597517.

rs1415755975 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:54000038 (GRCh38)
8:54912598 (GRCh37)
Canonical SPDI:: NC_000008.11:54000037:C:T
Gene:: TCEA1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,non_coding_transcript_variant,coding_sequence_variant,missense_variant
HGVS:: NC_000008.11:g.54000038C>T, NC_000008.10:g.54912598C>T, NM_006756.4:c.139G>A, NM_006756.3:c.139G>A, NM_006756.2:c.139G>A, NM_201437.3:c.76G>A, NM_201437.2:c.76G>A, NM_201437.1:c.76G>A, NR_109901.2:n.663G>A, NR_109901.1:n.671G>A, XM_011517578.2:c.34G>A, XM_011517578.1:c.34G>A, XM_006716467.2:c.-3G>A, XM_006716467.1:c.-3G>A, NP_006747.1:p.Gly47Arg, NP_958845.1:p.Gly26Arg, XP_011515880.1:p.Gly12Arg

Select item 140582559318.

rs1405825593 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 8:54022092 (GRCh38)
8:54934652 (GRCh37)
Canonical SPDI:: NC_000008.11:54022091:T:A,NC_000008.11:54022091:T:C
Gene:: TCEA1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
A=0.000106/3 (TOMMO)
HGVS:: NC_000008.11:g.54022092T>A, NC_000008.11:g.54022092T>C, NC_000008.10:g.54934652T>A, NC_000008.10:g.54934652T>C, NM_006756.4:c.34A>T, NM_006756.4:c.34A>G, NM_006756.3:c.34A>T, NM_006756.3:c.34A>G, NM_006756.2:c.34A>T, NM_006756.2:c.34A>G, NM_201437.3:c.34A>T, NM_201437.3:c.34A>G, NM_201437.2:c.34A>T, NM_201437.2:c.34A>G, NM_201437.1:c.34A>T, NM_201437.1:c.34A>G, NR_109901.2:n.357A>T, NR_109901.2:n.357A>G, NR_109901.1:n.365A>T, NR_109901.1:n.365A>G, XM_006716467.2:c.-157A>T, XM_006716467.2:c.-157A>G, XM_006716467.1:c.-157A>T, XM_006716467.1:c.-157A>G, NR_109902.2:n.357A>T, NR_109902.2:n.357A>G, NR_109902.1:n.365A>T, NR_109902.1:n.365A>G, NP_006747.1:p.Met12Leu, NP_006747.1:p.Met12Val, NP_958845.1:p.Met12Leu, NP_958845.1:p.Met12Val

Select item 140369590419.

rs1403695904 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:53993751 (GRCh38)
8:54906311 (GRCh37)
Canonical SPDI:: NC_000008.11:53993750:C:T
Gene:: TCEA1 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53993751C>T, NC_000008.10:g.54906311C>T, NM_006756.4:c.237G>A, NM_006756.3:c.237G>A, NM_006756.2:c.237G>A, NM_201437.3:c.174G>A, NM_201437.2:c.174G>A, NM_201437.1:c.174G>A, NR_109901.2:n.761G>A, NR_109901.1:n.769G>A, XM_011517578.2:c.132G>A, XM_011517578.1:c.132G>A, XM_006716467.2:c.96G>A, XM_006716467.1:c.96G>A

Select item 140140021320.

rs1401400213 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:53988233 (GRCh38)
8:54900793 (GRCh37)
Canonical SPDI:: NC_000008.11:53988232:C:A
Gene:: TCEA1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.53988233C>A, NC_000008.10:g.54900793C>A, NM_006756.4:c.347G>T, NM_006756.3:c.347G>T, NM_006756.2:c.347G>T, NM_201437.3:c.284G>T, NM_201437.2:c.284G>T, NM_201437.1:c.284G>T, NR_109901.2:n.871G>T, NR_109901.1:n.879G>T, XM_011517578.2:c.242G>T, XM_011517578.1:c.242G>T, XM_006716467.2:c.206G>T, XM_006716467.1:c.206G>T, NP_006747.1:p.Arg116Ile, NP_958845.1:p.Arg95Ile, XP_011515880.1:p.Arg81Ile, XP_006716530.1:p.Arg69Ile

<< First< Prev

Page of 12

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Protein (Select 45439355) (227)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: