SNP Links for Protein (Select 749385047) - SNP

Links from Protein

Items: 1 to 20 of 156

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Select item 14873382531.

rs1487338253 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:42404050 (GRCh38)
3:42445542 (GRCh37)
Canonical SPDI:: NC_000003.12:42404049:C:T
Gene:: LYZL4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42404050C>T, NC_000003.11:g.42445542C>T, XM_011533355.4:c.367G>A, XM_011533355.3:c.367G>A, XM_011533355.2:c.367G>A, XM_011533355.1:c.367G>A, NM_144634.4:c.367G>A, NM_144634.3:c.367G>A, NM_144634.2:c.367G>A, NM_001304386.2:c.367G>A, NM_001304386.1:c.367G>A, XP_011531657.1:p.Ala123Thr, NP_653235.1:p.Ala123Thr, NP_001291315.1:p.Ala123Thr

Select item 14866580072.

rs1486658007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:42407170 (GRCh38)
3:42448662 (GRCh37)
Canonical SPDI:: NC_000003.12:42407169:C:A
Gene:: LYZL4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42407170C>A, NC_000003.11:g.42448662C>A, XM_011533355.4:c.82G>T, XM_011533355.3:c.82G>T, XM_011533355.2:c.82G>T, XM_011533355.1:c.82G>T, NM_144634.4:c.82G>T, NM_144634.3:c.82G>T, NM_144634.2:c.82G>T, NM_001304386.2:c.82G>T, NM_001304386.1:c.82G>T, XP_011531657.1:p.Ala28Ser, NP_653235.1:p.Ala28Ser, NP_001291315.1:p.Ala28Ser

Select item 14765890443.

rs1476589044 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 3:42407184 (GRCh38)
3:42448676 (GRCh37)
Canonical SPDI:: NC_000003.12:42407183:C:G
Gene:: LYZL4 (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_000003.12:g.42407184C>G, NC_000003.11:g.42448676C>G, XM_011533355.4:c.68G>C, XM_011533355.3:c.68G>C, XM_011533355.2:c.68G>C, XM_011533355.1:c.68G>C, NM_144634.4:c.68G>C, NM_144634.3:c.68G>C, NM_144634.2:c.68G>C, NM_001304386.2:c.68G>C, NM_001304386.1:c.68G>C, XP_011531657.1:p.Gly23Ala, NP_653235.1:p.Gly23Ala, NP_001291315.1:p.Gly23Ala

Select item 14735059404.

rs1473505940 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:42406913 (GRCh38)
3:42448405 (GRCh37)
Canonical SPDI:: NC_000003.12:42406912:G:A
Gene:: LYZL4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000003.12:g.42406913G>A, NC_000003.11:g.42448405G>A, XM_011533355.4:c.225C>T, XM_011533355.3:c.225C>T, XM_011533355.2:c.225C>T, XM_011533355.1:c.225C>T, NM_144634.4:c.225C>T, NM_144634.3:c.225C>T, NM_144634.2:c.225C>T, NM_001304386.2:c.225C>T, NM_001304386.1:c.225C>T

Select item 14720302875.

rs1472030287 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:42407176 (GRCh38)
3:42448668 (GRCh37)
Canonical SPDI:: NC_000003.12:42407175:T:C
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.42407176T>C, NC_000003.11:g.42448668T>C, XM_011533355.4:c.76A>G, XM_011533355.3:c.76A>G, XM_011533355.2:c.76A>G, XM_011533355.1:c.76A>G, NM_144634.4:c.76A>G, NM_144634.3:c.76A>G, NM_144634.2:c.76A>G, NM_001304386.2:c.76A>G, NM_001304386.1:c.76A>G, XP_011531657.1:p.Thr26Ala, NP_653235.1:p.Thr26Ala, NP_001291315.1:p.Thr26Ala

Select item 14554283596.

rs1455428359 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:42406889 (GRCh38)
3:42448381 (GRCh37)
Canonical SPDI:: NC_000003.12:42406888:C:A
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000003.12:g.42406889C>A, NC_000003.11:g.42448381C>A, XM_011533355.4:c.249G>T, XM_011533355.3:c.249G>T, XM_011533355.2:c.249G>T, XM_011533355.1:c.249G>T, NM_144634.4:c.249G>T, NM_144634.3:c.249G>T, NM_144634.2:c.249G>T, NM_001304386.2:c.249G>T, NM_001304386.1:c.249G>T, XP_011531657.1:p.Trp83Cys, NP_653235.1:p.Trp83Cys, NP_001291315.1:p.Trp83Cys

Select item 14326274127.

rs1432627412 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:42407151 (GRCh38)
3:42448643 (GRCh37)
Canonical SPDI:: NC_000003.12:42407150:C:T
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_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_000003.12:g.42407151C>T, NC_000003.11:g.42448643C>T, XM_011533355.4:c.101G>A, XM_011533355.3:c.101G>A, XM_011533355.2:c.101G>A, XM_011533355.1:c.101G>A, NM_144634.4:c.101G>A, NM_144634.3:c.101G>A, NM_144634.2:c.101G>A, NM_001304386.2:c.101G>A, NM_001304386.1:c.101G>A, XP_011531657.1:p.Gly34Glu, NP_653235.1:p.Gly34Glu, NP_001291315.1:p.Gly34Glu

Select item 14130552218.

rs1413055221 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:42397270 (GRCh38)
3:42438762 (GRCh37)
Canonical SPDI:: NC_000003.12:42397269:G:T
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000003.12:g.42397270G>T, NC_000003.11:g.42438762G>T, NM_144634.4:c.436C>A, NM_144634.3:c.436C>A, NM_144634.2:c.436C>A, NM_001304386.2:c.436C>A, NM_001304386.1:c.436C>A, NP_653235.1:p.Leu146Met, NP_001291315.1:p.Leu146Met

Select item 14039002739.

rs1403900273 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:42407113 (GRCh38)
3:42448605 (GRCh37)
Canonical SPDI:: NC_000003.12:42407112:A:G
Gene:: LYZL4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42407113A>G, NC_000003.11:g.42448605A>G, XM_011533355.4:c.139T>C, XM_011533355.3:c.139T>C, XM_011533355.2:c.139T>C, XM_011533355.1:c.139T>C, NM_144634.4:c.139T>C, NM_144634.3:c.139T>C, NM_144634.2:c.139T>C, NM_001304386.2:c.139T>C, NM_001304386.1:c.139T>C, XP_011531657.1:p.Trp47Arg, NP_653235.1:p.Trp47Arg, NP_001291315.1:p.Trp47Arg

Select item 140194707910.

rs1401947079 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:42406856 (GRCh38)
3:42448348 (GRCh37)
Canonical SPDI:: NC_000003.12:42406855:C:T
Gene:: LYZL4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.42406856C>T, NC_000003.11:g.42448348C>T, XM_011533355.4:c.282G>A, XM_011533355.3:c.282G>A, XM_011533355.2:c.282G>A, XM_011533355.1:c.282G>A, NM_144634.4:c.282G>A, NM_144634.3:c.282G>A, NM_144634.2:c.282G>A, NM_001304386.2:c.282G>A, NM_001304386.1:c.282G>A, XP_011531657.1:p.Met94Ile, NP_653235.1:p.Met94Ile, NP_001291315.1:p.Met94Ile

Select item 139906716211.

rs1399067162 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:42404061 (GRCh38)
3:42445553 (GRCh37)
Canonical SPDI:: NC_000003.12:42404060:T:C
Gene:: LYZL4 (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_000003.12:g.42404061T>C, NC_000003.11:g.42445553T>C, XM_011533355.4:c.356A>G, XM_011533355.3:c.356A>G, XM_011533355.2:c.356A>G, XM_011533355.1:c.356A>G, NM_144634.4:c.356A>G, NM_144634.3:c.356A>G, NM_144634.2:c.356A>G, NM_001304386.2:c.356A>G, NM_001304386.1:c.356A>G, XP_011531657.1:p.Glu119Gly, NP_653235.1:p.Glu119Gly, NP_001291315.1:p.Glu119Gly

Select item 136834746612.

rs1368347466 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:42407174 (GRCh38)
3:42448666 (GRCh37)
Canonical SPDI:: NC_000003.12:42407173:T:G
Gene:: LYZL4 (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)
HGVS:: NC_000003.12:g.42407174T>G, NC_000003.11:g.42448666T>G, XM_011533355.4:c.78A>C, XM_011533355.3:c.78A>C, XM_011533355.2:c.78A>C, XM_011533355.1:c.78A>C, NM_144634.4:c.78A>C, NM_144634.3:c.78A>C, NM_144634.2:c.78A>C, NM_001304386.2:c.78A>C, NM_001304386.1:c.78A>C

Select item 136816723413.

rs1368167234 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:42407189 (GRCh38)
3:42448681 (GRCh37)
Canonical SPDI:: NC_000003.12:42407188:G:T
Gene:: LYZL4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42407189G>T, NC_000003.11:g.42448681G>T, XM_011533355.4:c.63C>A, XM_011533355.3:c.63C>A, XM_011533355.2:c.63C>A, XM_011533355.1:c.63C>A, NM_144634.4:c.63C>A, NM_144634.3:c.63C>A, NM_144634.2:c.63C>A, NM_001304386.2:c.63C>A, NM_001304386.1:c.63C>A

Select item 136348434414.

rs1363484344 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:42406901 (GRCh38)
3:42448393 (GRCh37)
Canonical SPDI:: NC_000003.12:42406900:A:G
Gene:: LYZL4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42406901A>G, NC_000003.11:g.42448393A>G, XM_011533355.4:c.237T>C, XM_011533355.3:c.237T>C, XM_011533355.2:c.237T>C, XM_011533355.1:c.237T>C, NM_144634.4:c.237T>C, NM_144634.3:c.237T>C, NM_144634.2:c.237T>C, NM_001304386.2:c.237T>C, NM_001304386.1:c.237T>C

Select item 135587621515.

rs1355876215 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:42407122 (GRCh38)
3:42448614 (GRCh37)
Canonical SPDI:: NC_000003.12:42407121:G:C
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000019/5 (TOPMED)
HGVS:: NC_000003.12:g.42407122G>C, NC_000003.11:g.42448614G>C, XM_011533355.4:c.130C>G, XM_011533355.3:c.130C>G, XM_011533355.2:c.130C>G, XM_011533355.1:c.130C>G, NM_144634.4:c.130C>G, NM_144634.3:c.130C>G, NM_144634.2:c.130C>G, NM_001304386.2:c.130C>G, NM_001304386.1:c.130C>G, XP_011531657.1:p.Leu44Val, NP_653235.1:p.Leu44Val, NP_001291315.1:p.Leu44Val

Select item 135017877216.

rs1350178772 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:42407215 (GRCh38)
3:42448707 (GRCh37)
Canonical SPDI:: NC_000003.12:42407214:G:A
Gene:: LYZL4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42407215G>A, NC_000003.11:g.42448707G>A, XM_011533355.4:c.37C>T, XM_011533355.3:c.37C>T, XM_011533355.2:c.37C>T, XM_011533355.1:c.37C>T, NM_144634.4:c.37C>T, NM_144634.3:c.37C>T, NM_144634.2:c.37C>T, NM_001304386.2:c.37C>T, NM_001304386.1:c.37C>T

Select item 134811944617.

rs1348119446 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:42406915 (GRCh38)
3:42448407 (GRCh37)
Canonical SPDI:: NC_000003.12:42406914:G:A
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000043/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.42406915G>A, NC_000003.11:g.42448407G>A, XM_011533355.4:c.223C>T, XM_011533355.3:c.223C>T, XM_011533355.2:c.223C>T, XM_011533355.1:c.223C>T, NM_144634.4:c.223C>T, NM_144634.3:c.223C>T, NM_144634.2:c.223C>T, NM_001304386.2:c.223C>T, NM_001304386.1:c.223C>T, XP_011531657.1:p.Leu75Phe, NP_653235.1:p.Leu75Phe, NP_001291315.1:p.Leu75Phe

Select item 134751220018.

rs1347512200 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 3:42406887 (GRCh38)
3:42448379 (GRCh37)
Canonical SPDI:: NC_000003.12:42406886:C:G,NC_000003.12:42406886:C:T
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42406887C>G, NC_000003.12:g.42406887C>T, NC_000003.11:g.42448379C>G, NC_000003.11:g.42448379C>T, XM_011533355.4:c.251G>C, XM_011533355.4:c.251G>A, XM_011533355.3:c.251G>C, XM_011533355.3:c.251G>A, XM_011533355.2:c.251G>C, XM_011533355.2:c.251G>A, XM_011533355.1:c.251G>C, XM_011533355.1:c.251G>A, NM_144634.4:c.251G>C, NM_144634.4:c.251G>A, NM_144634.3:c.251G>C, NM_144634.3:c.251G>A, NM_144634.2:c.251G>C, NM_144634.2:c.251G>A, NM_001304386.2:c.251G>C, NM_001304386.2:c.251G>A, NM_001304386.1:c.251G>C, NM_001304386.1:c.251G>A, XP_011531657.1:p.Cys84Ser, XP_011531657.1:p.Cys84Tyr, NP_653235.1:p.Cys84Ser, NP_653235.1:p.Cys84Tyr, NP_001291315.1:p.Cys84Ser, NP_001291315.1:p.Cys84Tyr

Select item 134092033119.

rs1340920331 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 3:42407221 (GRCh38)
3:42448713 (GRCh37)
Canonical SPDI:: NC_000003.12:42407220:C:A
Gene:: LYZL4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.42407221C>A, NC_000003.11:g.42448713C>A, XM_011533355.4:c.31G>T, XM_011533355.3:c.31G>T, XM_011533355.2:c.31G>T, XM_011533355.1:c.31G>T, NM_144634.4:c.31G>T, NM_144634.3:c.31G>T, NM_144634.2:c.31G>T, NM_001304386.2:c.31G>T, NM_001304386.1:c.31G>T, XP_011531657.1:p.Gly11Cys, NP_653235.1:p.Gly11Cys, NP_001291315.1:p.Gly11Cys

Select item 134061024520.

rs1340610245 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 3:42406972 (GRCh38)
3:42448464 (GRCh37)
Canonical SPDI:: NC_000003.12:42406971:T:A
Gene:: LYZL4 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.42406972T>A, NC_000003.11:g.42448464T>A, XM_011533355.4:c.166A>T, XM_011533355.3:c.166A>T, XM_011533355.2:c.166A>T, XM_011533355.1:c.166A>T, NM_144634.4:c.166A>T, NM_144634.3:c.166A>T, NM_144634.2:c.166A>T, NM_001304386.2:c.166A>T, NM_001304386.1:c.166A>T, XP_011531657.1:p.Lys56Ter, NP_653235.1:p.Lys56Ter, NP_001291315.1:p.Lys56Ter

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