SNP Links for Protein (Select 317008577) - SNP

Links from Protein

Items: 1 to 20 of 154

<< First< Prev

Page of 8

Next >Last >>

Select item 14905571481.

rs1490557148 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:35936798 (GRCh38)
17:34263802 (GRCh37)
Canonical SPDI:: NC_000017.11:35936797:A:G
Gene:: LYZL6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.35936798A>G, NT_187614.1:g.171330A>G, NC_000017.10:g.34263802A>G, NM_020426.4:c.334T>C, NM_020426.3:c.334T>C, NM_020426.2:c.334T>C, NM_001199951.3:c.334T>C, NM_001199951.2:c.334T>C, NM_001199951.1:c.334T>C, NP_065159.1:p.Cys112Arg, NP_001186880.1:p.Cys112Arg

Select item 14767220322.

rs1476722032 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:35937836 (GRCh38)
17:34264840 (GRCh37)
Canonical SPDI:: NC_000017.11:35937835:G:A
Gene:: LYZL6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.35937836G>A, NT_187614.1:g.172368G>A, NC_000017.10:g.34264840G>A, NM_020426.4:c.220C>T, NM_020426.3:c.220C>T, NM_020426.2:c.220C>T, NM_001199951.3:c.220C>T, NM_001199951.2:c.220C>T, NM_001199951.1:c.220C>T, NP_065159.1:p.Leu74Phe, NP_001186880.1:p.Leu74Phe

Select item 14741207073.

rs1474120707 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 17:35937794 (GRCh38)
17:34264798 (GRCh37)
Canonical SPDI:: NC_000017.11:35937793:T:G
Gene:: LYZL6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000017.11:g.35937794T>G, NT_187614.1:g.172326T>G, NC_000017.10:g.34264798T>G, NM_020426.4:c.262A>C, NM_020426.3:c.262A>C, NM_020426.2:c.262A>C, NM_001199951.3:c.262A>C, NM_001199951.2:c.262A>C, NM_001199951.1:c.262A>C, NP_065159.1:p.Ser88Arg, NP_001186880.1:p.Ser88Arg

Select item 14692880904.

rs1469288090 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:35937847 (GRCh38)
17:34264851 (GRCh37)
Canonical SPDI:: NC_000017.11:35937846:A:G
Gene:: LYZL6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.35937847A>G, NT_187614.1:g.172379A>G, NC_000017.10:g.34264851A>G, NM_020426.4:c.209T>C, NM_020426.3:c.209T>C, NM_020426.2:c.209T>C, NM_001199951.3:c.209T>C, NM_001199951.2:c.209T>C, NM_001199951.1:c.209T>C, NP_065159.1:p.Phe70Ser, NP_001186880.1:p.Phe70Ser

Select item 14627352795.

rs1462735279 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:35939297 (GRCh38)
17:34266301 (GRCh37)
Canonical SPDI:: NC_000017.11:35939296:G:A
Gene:: LYZL6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.35939297G>A, NT_187614.1:g.173829G>A, NC_000017.10:g.34266301G>A, NM_020426.4:c.60C>T, NM_020426.3:c.60C>T, NM_020426.2:c.60C>T, NM_001199951.3:c.60C>T, NM_001199951.2:c.60C>T, NM_001199951.1:c.60C>T

Select item 14626677166.

rs1462667716 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->C [Show Flanks]
Chromosome:: 17:35934852 (GRCh38)
17:34261857 (GRCh37)
Canonical SPDI:: NC_000017.11:35934852:CC:CCC
Gene:: LYZL6 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CCC=0./0 (ALFA)
HGVS:: NC_000017.11:g.35934854dup, NT_187614.1:g.169386dup, NC_000017.10:g.34261858dup, NM_020426.4:c.390dup, NM_020426.3:c.390dup, NM_020426.2:c.390dup, NM_001199951.3:c.390dup, NM_001199951.2:c.390dup, NM_001199951.1:c.390dup, NP_065159.1:p.Leu131fs, NP_001186880.1:p.Leu131fs

Select item 14541282967.

rs1454128296 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:35939342 (GRCh38)
17:34266346 (GRCh37)
Canonical SPDI:: NC_000017.11:35939341:T:C
Gene:: LYZL6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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.35939342T>C, NT_187614.1:g.173874T>C, NC_000017.10:g.34266346T>C, NM_020426.4:c.15A>G, NM_020426.3:c.15A>G, NM_020426.2:c.15A>G, NM_001199951.3:c.15A>G, NM_001199951.2:c.15A>G, NM_001199951.1:c.15A>G

Select item 14540444478.

rs1454044447 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:35934846 (GRCh38)
17:34261850 (GRCh37)
Canonical SPDI:: NC_000017.11:35934845:A:G
Gene:: LYZL6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.35934846A>G, NT_187614.1:g.169378A>G, NC_000017.10:g.34261850A>G, NM_020426.4:c.397T>C, NM_020426.3:c.397T>C, NM_020426.2:c.397T>C, NM_001199951.3:c.397T>C, NM_001199951.2:c.397T>C, NM_001199951.1:c.397T>C, NP_065159.1:p.Cys133Arg, NP_001186880.1:p.Cys133Arg

Select item 14501334849.

rs1450133484 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35939255 (GRCh38)
17:34266259 (GRCh37)
Canonical SPDI:: NC_000017.11:35939254:C:T
Gene:: LYZL6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000017.11:g.35939255C>T, NT_187614.1:g.173787C>T, NC_000017.10:g.34266259C>T, NM_020426.4:c.102G>A, NM_020426.3:c.102G>A, NM_020426.2:c.102G>A, NM_001199951.3:c.102G>A, NM_001199951.2:c.102G>A, NM_001199951.1:c.102G>A

Select item 144283759010.

rs1442837590 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:35934829 (GRCh38)
17:34261833 (GRCh37)
Canonical SPDI:: NC_000017.11:35934828:G:A,NC_000017.11:35934828:G:T
Gene:: LYZL6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.35934829G>A, NC_000017.11:g.35934829G>T, NT_187614.1:g.169361G>A, NT_187614.1:g.169361G>T, NC_000017.10:g.34261833G>A, NC_000017.10:g.34261833G>T, NM_020426.4:c.414C>T, NM_020426.4:c.414C>A, NM_020426.3:c.414C>T, NM_020426.3:c.414C>A, NM_020426.2:c.414C>T, NM_020426.2:c.414C>A, NM_001199951.3:c.414C>T, NM_001199951.3:c.414C>A, NM_001199951.2:c.414C>T, NM_001199951.2:c.414C>A, NM_001199951.1:c.414C>T, NM_001199951.1:c.414C>A

Select item 143815063811.

rs1438150638 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35939276 (GRCh38)
17:34266280 (GRCh37)
Canonical SPDI:: NC_000017.11:35939275:C:T
Gene:: LYZL6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000017.11:g.35939276C>T, NT_187614.1:g.173808C>T, NC_000017.10:g.34266280C>T, NM_020426.4:c.81G>A, NM_020426.3:c.81G>A, NM_020426.2:c.81G>A, NM_001199951.3:c.81G>A, NM_001199951.2:c.81G>A, NM_001199951.1:c.81G>A

Select item 142911556012.

rs1429115560 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 17:35936803 (GRCh38)
17:34263807 (GRCh37)
Canonical SPDI:: NC_000017.11:35936802:A:T
Gene:: LYZL6 (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_000017.11:g.35936803A>T, NT_187614.1:g.171335A>T, NC_000017.10:g.34263807A>T, NM_020426.4:c.329T>A, NM_020426.3:c.329T>A, NM_020426.2:c.329T>A, NM_001199951.3:c.329T>A, NM_001199951.2:c.329T>A, NM_001199951.1:c.329T>A, NP_065159.1:p.Ile110Asn, NP_001186880.1:p.Ile110Asn

Select item 139146910913.

rs1391469109 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:35937872 (GRCh38)
17:34264876 (GRCh37)
Canonical SPDI:: NC_000017.11:35937871:T:C
Gene:: LYZL6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.35937872T>C, NT_187614.1:g.172404T>C, NC_000017.10:g.34264876T>C, NM_020426.4:c.184A>G, NM_020426.3:c.184A>G, NM_020426.2:c.184A>G, NM_001199951.3:c.184A>G, NM_001199951.2:c.184A>G, NM_001199951.1:c.184A>G, NP_065159.1:p.Ile62Val, NP_001186880.1:p.Ile62Val

Select item 138713014914.

rs1387130149 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:35937766 (GRCh38)
17:34264770 (GRCh37)
Canonical SPDI:: NC_000017.11:35937765:T:C
Gene:: LYZL6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.35937766T>C, NT_187614.1:g.172298T>C, NC_000017.10:g.34264770T>C, NM_020426.4:c.290A>G, NM_020426.3:c.290A>G, NM_020426.2:c.290A>G, NM_001199951.3:c.290A>G, NM_001199951.2:c.290A>G, NM_001199951.1:c.290A>G, NP_065159.1:p.Asp97Gly, NP_001186880.1:p.Asp97Gly

Select item 138146665015.

rs1381466650 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35934854 (GRCh38)
17:34261858 (GRCh37)
Canonical SPDI:: NC_000017.11:35934853:C:T
Gene:: LYZL6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.35934854C>T, NT_187614.1:g.169386C>T, NC_000017.10:g.34261858C>T, NM_020426.4:c.389G>A, NM_020426.3:c.389G>A, NM_020426.2:c.389G>A, NM_001199951.3:c.389G>A, NM_001199951.2:c.389G>A, NM_001199951.1:c.389G>A, NP_065159.1:p.Arg130Lys, NP_001186880.1:p.Arg130Lys

Select item 136688030016.

rs1366880300 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:35936822 (GRCh38)
17:34263826 (GRCh37)
Canonical SPDI:: NC_000017.11:35936821:G:A
Gene:: LYZL6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.35936822G>A, NT_187614.1:g.171354G>A, NC_000017.10:g.34263826G>A, NM_020426.4:c.310C>T, NM_020426.3:c.310C>T, NM_020426.2:c.310C>T, NM_001199951.3:c.310C>T, NM_001199951.2:c.310C>T, NM_001199951.1:c.310C>T, NP_065159.1:p.Pro104Ser, NP_001186880.1:p.Pro104Ser

Select item 136389260917.

rs1363892609 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 17:35939308 (GRCh38)
17:34266312 (GRCh37)
Canonical SPDI:: NC_000017.11:35939307:T:A,NC_000017.11:35939307:T:G
Gene:: LYZL6 (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)
HGVS:: NC_000017.11:g.35939308T>A, NC_000017.11:g.35939308T>G, NT_187614.1:g.173840T>A, NT_187614.1:g.173840T>G, NC_000017.10:g.34266312T>A, NC_000017.10:g.34266312T>G, NM_020426.4:c.49A>T, NM_020426.4:c.49A>C, NM_020426.3:c.49A>T, NM_020426.3:c.49A>C, NM_020426.2:c.49A>T, NM_020426.2:c.49A>C, NM_001199951.3:c.49A>T, NM_001199951.3:c.49A>C, NM_001199951.2:c.49A>T, NM_001199951.2:c.49A>C, NM_001199951.1:c.49A>T, NM_001199951.1:c.49A>C, NP_065159.1:p.Asn17Tyr, NP_065159.1:p.Asn17His, NP_001186880.1:p.Asn17Tyr, NP_001186880.1:p.Asn17His

Select item 135513607618.

rs1355136076 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35939269 (GRCh38)
17:34266273 (GRCh37)
Canonical SPDI:: NC_000017.11:35939268:C:T
Gene:: LYZL6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.35939269C>T, NT_187614.1:g.173801C>T, NC_000017.10:g.34266273C>T, NM_020426.4:c.88G>A, NM_020426.3:c.88G>A, NM_020426.2:c.88G>A, NM_001199951.3:c.88G>A, NM_001199951.2:c.88G>A, NM_001199951.1:c.88G>A, NP_065159.1:p.Val30Met, NP_001186880.1:p.Val30Met

Select item 134526905019.

rs1345269050 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:35937897 (GRCh38)
17:34264901 (GRCh37)
Canonical SPDI:: NC_000017.11:35937896:C:T
Gene:: LYZL6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.35937897C>T, NT_187614.1:g.172429C>T, NC_000017.10:g.34264901C>T, NM_020426.4:c.159G>A, NM_020426.3:c.159G>A, NM_020426.2:c.159G>A, NM_001199951.3:c.159G>A, NM_001199951.2:c.159G>A, NM_001199951.1:c.159G>A

Select item 132988600220.

rs1329886002 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:35939231 (GRCh38)
17:34266235 (GRCh37)
Canonical SPDI:: NC_000017.11:35939230:G:A
Gene:: LYZL6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.00002/5 (GnomAD_exomes)
HGVS:: NC_000017.11:g.35939231G>A, NT_187614.1:g.173763G>A, NC_000017.10:g.34266235G>A, NM_020426.4:c.126C>T, NM_020426.3:c.126C>T, NM_020426.2:c.126C>T, NM_001199951.3:c.126C>T, NM_001199951.2:c.126C>T, NM_001199951.1:c.126C>T

<< First< Prev

Page of 8

Next >Last >>

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 154

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity