SNP Links for Protein (Select 50845399) - SNP

Links from Protein

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Select item 14878356171.

rs1487835617 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 6:31671226 (GRCh38)
6:31639003 (GRCh37)
Canonical SPDI:: NC_000006.12:31671225:C:G,NC_000006.12:31671225:C:T
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31671226C>G, NC_000006.12:g.31671226C>T, NC_000006.11:g.31639003C>G, NC_000006.11:g.31639003C>T, NT_113891.3:g.3148517C>G, NT_113891.3:g.3148517C>T, NT_113891.2:g.3148623C>G, NT_113891.2:g.3148623C>T, NT_167248.2:g.2927050C>G, NT_167248.2:g.2927050C>T, NT_167248.1:g.2932646C>G, NT_167248.1:g.2932646C>T, NT_167245.2:g.2918998C>G, NT_167245.2:g.2918998C>T, NT_167245.1:g.2924583C>G, NT_167245.1:g.2924583C>T, NT_167249.2:g.2970510C>G, NT_167249.2:g.2970510C>T, NT_167249.1:g.2969808C>G, NT_167249.1:g.2969808C>T, NT_167246.2:g.2976273C>G, NT_167246.2:g.2976273C>T, NT_167246.1:g.2981893C>G, NT_167246.1:g.2981893C>T, NT_167247.2:g.3013098C>G, NT_167247.2:g.3013098C>T, NT_167247.1:g.3018683C>G, NT_167247.1:g.3018683C>T, NM_021221.3:c.129C>G, NM_021221.3:c.129C>T, NM_021221.2:c.129C>G, NM_021221.2:c.129C>T

Select item 14869309032.

rs1486930903 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31670955 (GRCh38)
6:31638732 (GRCh37)
Canonical SPDI:: NC_000006.12:31670954:A:G
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.31670955A>G, NC_000006.11:g.31638732A>G, NT_113891.3:g.3148246A>G, NT_113891.2:g.3148352A>G, NT_167248.2:g.2926779A>G, NT_167248.1:g.2932375A>G, NT_167245.2:g.2918727A>G, NT_167245.1:g.2924312A>G, NT_167249.2:g.2970239A>G, NT_167249.1:g.2969537A>G, NT_167246.2:g.2976002A>G, NT_167246.1:g.2981622A>G, NT_167247.2:g.3012827A>G, NT_167247.1:g.3018412A>G, NM_021221.3:c.5A>G, NM_021221.2:c.5A>G, NP_067044.2:p.Lys2Arg

Select item 14822586483.

rs1482258648 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31671204 (GRCh38)
6:31638981 (GRCh37)
Canonical SPDI:: NC_000006.12:31671203:C:T
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.31671204C>T, NC_000006.11:g.31638981C>T, NT_113891.3:g.3148495C>T, NT_113891.2:g.3148601C>T, NT_167248.2:g.2927028C>T, NT_167248.1:g.2932624C>T, NT_167245.2:g.2918976C>T, NT_167245.1:g.2924561C>T, NT_167249.2:g.2970488C>T, NT_167249.1:g.2969786C>T, NT_167246.2:g.2976251C>T, NT_167246.1:g.2981871C>T, NT_167247.2:g.3013076C>T, NT_167247.1:g.3018661C>T, NM_021221.3:c.107C>T, NM_021221.2:c.107C>T, NP_067044.2:p.Pro36Leu

Select item 14778815154.

rs1477881515 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31671265 (GRCh38)
6:31639042 (GRCh37)
Canonical SPDI:: NC_000006.12:31671264:G:A
Gene:: LY6G5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000021/3 (GnomAD)
A=0.000625/4 (1000Genomes)
HGVS:: NC_000006.12:g.31671265G>A, NC_000006.11:g.31639042G>A, NT_113891.3:g.3148556G>A, NT_113891.2:g.3148662G>A, NT_167248.2:g.2927089G>A, NT_167248.1:g.2932685G>A, NT_167245.2:g.2919037G>A, NT_167245.1:g.2924622G>A, NT_167249.2:g.2970549G>A, NT_167249.1:g.2969847G>A, NT_167246.2:g.2976312G>A, NT_167246.1:g.2981932G>A, NT_167247.2:g.3013137G>A, NT_167247.1:g.3018722G>A, NM_021221.3:c.168G>A, NM_021221.2:c.168G>A, NP_067044.2:p.Met56Ile

Select item 14726598495.

rs1472659849 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:31672281 (GRCh38)
6:31640058 (GRCh37)
Canonical SPDI:: NC_000006.12:31672280:G:C
Gene:: LY6G5B (Varview)
Functional Consequence:: stop_lost,terminator_codon_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_000006.12:g.31672281G>C, NC_000006.11:g.31640058G>C, NT_113891.3:g.3149572G>C, NT_113891.2:g.3149678G>C, NT_167248.2:g.2928105G>C, NT_167248.1:g.2933701G>C, NT_167245.2:g.2920053G>C, NT_167245.1:g.2925638G>C, NT_167249.2:g.2971565G>C, NT_167249.1:g.2970863G>C, NT_167246.2:g.2977328G>C, NT_167246.1:g.2982948G>C, NT_167247.2:g.3014153G>C, NT_167247.1:g.3019738G>C, NM_021221.3:c.605G>C, NM_021221.2:c.605G>C, NP_067044.2:p.Ter202Ser

Select item 14701532676.

rs1470153267 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 6:31671912 (GRCh38)
6:31639689 (GRCh37)
Canonical SPDI:: NC_000006.12:31671911:A:C,NC_000006.12:31671911:A:G
Gene:: LY6G5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.31671912A>C, NC_000006.12:g.31671912A>G, NC_000006.11:g.31639689A>C, NC_000006.11:g.31639689A>G, NT_113891.3:g.3149203A>C, NT_113891.3:g.3149203A>G, NT_113891.2:g.3149309A>C, NT_113891.2:g.3149309A>G, NT_167248.2:g.2927736A>C, NT_167248.2:g.2927736A>G, NT_167248.1:g.2933332A>C, NT_167248.1:g.2933332A>G, NT_167245.2:g.2919684A>C, NT_167245.2:g.2919684A>G, NT_167245.1:g.2925269A>C, NT_167245.1:g.2925269A>G, NT_167249.2:g.2971196A>C, NT_167249.2:g.2971196A>G, NT_167249.1:g.2970494A>C, NT_167249.1:g.2970494A>G, NT_167246.2:g.2976959A>C, NT_167246.2:g.2976959A>G, NT_167246.1:g.2982579A>C, NT_167246.1:g.2982579A>G, NT_167247.2:g.3013784A>C, NT_167247.2:g.3013784A>G, NT_167247.1:g.3019369A>C, NT_167247.1:g.3019369A>G, NM_021221.3:c.236A>C, NM_021221.3:c.236A>G, NM_021221.2:c.236A>C, NM_021221.2:c.236A>G, NP_067044.2:p.Tyr79Ser, NP_067044.2:p.Tyr79Cys

Select item 14680816357.

rs1468081635 [Homo sapiens]

Variant type:: DEL
Alleles:: CACCA>- [Show Flanks]
Chromosome:: 6:31671271 (GRCh38)
6:31639048 (GRCh37)
Canonical SPDI:: NC_000006.12:31671270:CACCA:
Gene:: LY6G5B (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: -=0.00005/7 (GnomAD)
HGVS:: NC_000006.12:g.31671271_31671275del, NC_000006.11:g.31639048_31639052del, NT_113891.3:g.3148562_3148566del, NT_113891.2:g.3148668_3148672del, NT_167248.2:g.2927095_2927099del, NT_167248.1:g.2932691_2932695del, NT_167245.2:g.2919043_2919047del, NT_167245.1:g.2924628_2924632del, NT_167249.2:g.2970555_2970559del, NT_167249.1:g.2969853_2969857del, NT_167246.2:g.2976318_2976322del, NT_167246.1:g.2981938_2981942del, NT_167247.2:g.3013143_3013147del, NT_167247.1:g.3018728_3018732del, NM_021221.3:c.174_178del, NM_021221.2:c.174_178del, NP_067044.2:p.Thr59fs

Select item 14608639718.

rs1460863971 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31671949 (GRCh38)
6:31639726 (GRCh37)
Canonical SPDI:: NC_000006.12:31671948:G:A
Gene:: LY6G5B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000006.12:g.31671949G>A, NC_000006.11:g.31639726G>A, NT_113891.3:g.3149240G>A, NT_113891.2:g.3149346G>A, NT_167248.2:g.2927773G>A, NT_167248.1:g.2933369G>A, NT_167245.2:g.2919721G>A, NT_167245.1:g.2925306G>A, NT_167249.2:g.2971233G>A, NT_167249.1:g.2970531G>A, NT_167246.2:g.2976996G>A, NT_167246.1:g.2982616G>A, NT_167247.2:g.3013821G>A, NT_167247.1:g.3019406G>A, NM_021221.3:c.273G>A, NM_021221.2:c.273G>A

Select item 14528710149.

rs1452871014 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:31672007 (GRCh38)
6:31639784 (GRCh37)
Canonical SPDI:: NC_000006.12:31672006:C:G
Gene:: LY6G5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.31672007C>G, NC_000006.11:g.31639784C>G, NT_113891.3:g.3149298C>G, NT_113891.2:g.3149404C>G, NT_167248.2:g.2927831C>G, NT_167248.1:g.2933427C>G, NT_167245.2:g.2919779C>G, NT_167245.1:g.2925364C>G, NT_167249.2:g.2971291C>G, NT_167249.1:g.2970589C>G, NT_167246.2:g.2977054C>G, NT_167246.1:g.2982674C>G, NT_167247.2:g.3013879C>G, NT_167247.1:g.3019464C>G, NM_021221.3:c.331C>G, NM_021221.2:c.331C>G, NP_067044.2:p.Gln111Glu

Select item 145059479210.

rs1450594792 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:31671281 (GRCh38)
6:31639058 (GRCh37)
Canonical SPDI:: NC_000006.12:31671280:T:C
Gene:: LY6G5B (Varview)
Functional Consequence:: missense_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_000006.12:g.31671281T>C, NC_000006.11:g.31639058T>C, NT_113891.3:g.3148572T>C, NT_113891.2:g.3148678T>C, NT_167248.2:g.2927105T>C, NT_167248.1:g.2932701T>C, NT_167245.2:g.2919053T>C, NT_167245.1:g.2924638T>C, NT_167249.2:g.2970565T>C, NT_167249.1:g.2969863T>C, NT_167246.2:g.2976328T>C, NT_167246.1:g.2981948T>C, NT_167247.2:g.3013153T>C, NT_167247.1:g.3018738T>C, NM_021221.3:c.184T>C, NM_021221.2:c.184T>C, NP_067044.2:p.Tyr62His

Select item 144467691411.

rs1444676914 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31671936 (GRCh38)
6:31639713 (GRCh37)
Canonical SPDI:: NC_000006.12:31671935:C:T
Gene:: LY6G5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.31671936C>T, NC_000006.11:g.31639713C>T, NT_113891.3:g.3149227C>T, NT_113891.2:g.3149333C>T, NT_167248.2:g.2927760C>T, NT_167248.1:g.2933356C>T, NT_167245.2:g.2919708C>T, NT_167245.1:g.2925293C>T, NT_167249.2:g.2971220C>T, NT_167249.1:g.2970518C>T, NT_167246.2:g.2976983C>T, NT_167246.1:g.2982603C>T, NT_167247.2:g.3013808C>T, NT_167247.1:g.3019393C>T, NM_021221.3:c.260C>T, NM_021221.2:c.260C>T, NP_067044.2:p.Thr87Ile

Select item 144456044212.

rs1444560442 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:31672181 (GRCh38)
6:31639958 (GRCh37)
Canonical SPDI:: NC_000006.12:31672180:G:C
Gene:: LY6G5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.31672181G>C, NC_000006.11:g.31639958G>C, NT_113891.3:g.3149472G>C, NT_113891.2:g.3149578G>C, NT_167248.2:g.2928005G>C, NT_167248.1:g.2933601G>C, NT_167245.2:g.2919953G>C, NT_167245.1:g.2925538G>C, NT_167249.2:g.2971465G>C, NT_167249.1:g.2970763G>C, NT_167246.2:g.2977228G>C, NT_167246.1:g.2982848G>C, NT_167247.2:g.3014053G>C, NT_167247.1:g.3019638G>C, NM_021221.3:c.505G>C, NM_021221.2:c.505G>C, NP_067044.2:p.Gly169Arg

Select item 143766309813.

rs1437663098 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31672180 (GRCh38)
6:31639957 (GRCh37)
Canonical SPDI:: NC_000006.12:31672179:G:A
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.31672180G>A, NC_000006.11:g.31639957G>A, NT_113891.3:g.3149471G>A, NT_113891.2:g.3149577G>A, NT_167248.2:g.2928004G>A, NT_167248.1:g.2933600G>A, NT_167245.2:g.2919952G>A, NT_167245.1:g.2925537G>A, NT_167249.2:g.2971464G>A, NT_167249.1:g.2970762G>A, NT_167246.2:g.2977227G>A, NT_167246.1:g.2982847G>A, NT_167247.2:g.3014052G>A, NT_167247.1:g.3019637G>A, NM_021221.3:c.504G>A, NM_021221.2:c.504G>A

Select item 142941717514.

rs1429417175 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31672102 (GRCh38)
6:31639879 (GRCh37)
Canonical SPDI:: NC_000006.12:31672101:C:T
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.31672102C>T, NC_000006.11:g.31639879C>T, NT_113891.3:g.3149393C>T, NT_113891.2:g.3149499C>T, NT_167248.2:g.2927926C>T, NT_167248.1:g.2933522C>T, NT_167245.2:g.2919874C>T, NT_167245.1:g.2925459C>T, NT_167249.2:g.2971386C>T, NT_167249.1:g.2970684C>T, NT_167246.2:g.2977149C>T, NT_167246.1:g.2982769C>T, NT_167247.2:g.3013974C>T, NT_167247.1:g.3019559C>T, NM_021221.3:c.426C>T, NM_021221.2:c.426C>T

Select item 142433279815.

rs1424332798 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31672078 (GRCh38)
6:31639855 (GRCh37)
Canonical SPDI:: NC_000006.12:31672077:G:A
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000094/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.31672078G>A, NC_000006.11:g.31639855G>A, NT_113891.3:g.3149369G>A, NT_113891.2:g.3149475G>A, NT_167248.2:g.2927902G>A, NT_167248.1:g.2933498G>A, NT_167245.2:g.2919850G>A, NT_167245.1:g.2925435G>A, NT_167249.2:g.2971362G>A, NT_167249.1:g.2970660G>A, NT_167246.2:g.2977125G>A, NT_167246.1:g.2982745G>A, NT_167247.2:g.3013950G>A, NT_167247.1:g.3019535G>A, NM_021221.3:c.402G>A, NM_021221.2:c.402G>A

Select item 141872825816.

rs1418728258 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:31670977 (GRCh38)
6:31638754 (GRCh37)
Canonical SPDI:: NC_000006.12:31670976:G:A
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000006.12:g.31670977G>A, NC_000006.11:g.31638754G>A, NT_113891.3:g.3148268G>A, NT_113891.2:g.3148374G>A, NT_167248.2:g.2926801G>A, NT_167248.1:g.2932397G>A, NT_167245.2:g.2918749G>A, NT_167245.1:g.2924334G>A, NT_167249.2:g.2970261G>A, NT_167249.1:g.2969559G>A, NT_167246.2:g.2976024G>A, NT_167246.1:g.2981644G>A, NT_167247.2:g.3012849G>A, NT_167247.1:g.3018434G>A, NM_021221.3:c.27G>A, NM_021221.2:c.27G>A

Select item 141796075417.

rs1417960754 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 6:31672223 (GRCh38)
6:31640000 (GRCh37)
Canonical SPDI:: NC_000006.12:31672222:A:T
Gene:: LY6G5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000006.12:g.31672223A>T, NC_000006.11:g.31640000A>T, NT_113891.3:g.3149514A>T, NT_113891.2:g.3149620A>T, NT_167248.2:g.2928047A>T, NT_167248.1:g.2933643A>T, NT_167245.2:g.2919995A>T, NT_167245.1:g.2925580A>T, NT_167249.2:g.2971507A>T, NT_167249.1:g.2970805A>T, NT_167246.2:g.2977270A>T, NT_167246.1:g.2982890A>T, NT_167247.2:g.3014095A>T, NT_167247.1:g.3019680A>T, NM_021221.3:c.547A>T, NM_021221.2:c.547A>T, NP_067044.2:p.Asn183Tyr

Select item 141675465218.

rs1416754652 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31671250 (GRCh38)
6:31639027 (GRCh37)
Canonical SPDI:: NC_000006.12:31671249:C:T
Gene:: LY6G5B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.31671250C>T, NC_000006.11:g.31639027C>T, NT_113891.3:g.3148541C>T, NT_113891.2:g.3148647C>T, NT_167248.2:g.2927074C>T, NT_167248.1:g.2932670C>T, NT_167245.2:g.2919022C>T, NT_167245.1:g.2924607C>T, NT_167249.2:g.2970534C>T, NT_167249.1:g.2969832C>T, NT_167246.2:g.2976297C>T, NT_167246.1:g.2981917C>T, NT_167247.2:g.3013122C>T, NT_167247.1:g.3018707C>T, NM_021221.3:c.153C>T, NM_021221.2:c.153C>T

Select item 140971446119.

rs1409714461 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:31671214 (GRCh38)
6:31638991 (GRCh37)
Canonical SPDI:: NC_000006.12:31671213:A:G
Gene:: LY6G5B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.31671214A>G, NC_000006.11:g.31638991A>G, NT_113891.3:g.3148505A>G, NT_113891.2:g.3148611A>G, NT_167248.2:g.2927038A>G, NT_167248.1:g.2932634A>G, NT_167245.2:g.2918986A>G, NT_167245.1:g.2924571A>G, NT_167249.2:g.2970498A>G, NT_167249.1:g.2969796A>G, NT_167246.2:g.2976261A>G, NT_167246.1:g.2981881A>G, NT_167247.2:g.3013086A>G, NT_167247.1:g.3018671A>G, NM_021221.3:c.117A>G, NM_021221.2:c.117A>G

Select item 140833822820.

rs1408338228 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:31671952 (GRCh38)
6:31639729 (GRCh37)
Canonical SPDI:: NC_000006.12:31671951:C:T
Gene:: LY6G5B (Varview)
Functional Consequence:: 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_000006.12:g.31671952C>T, NC_000006.11:g.31639729C>T, NT_113891.3:g.3149243C>T, NT_113891.2:g.3149349C>T, NT_167248.2:g.2927776C>T, NT_167248.1:g.2933372C>T, NT_167245.2:g.2919724C>T, NT_167245.1:g.2925309C>T, NT_167249.2:g.2971236C>T, NT_167249.1:g.2970534C>T, NT_167246.2:g.2976999C>T, NT_167246.1:g.2982619C>T, NT_167247.2:g.3013824C>T, NT_167247.1:g.3019409C>T, NM_021221.3:c.276C>T, NM_021221.2:c.276C>T

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