SNP Links for Protein (Select 4557251) - SNP

Links from Protein

Items: 1 to 20 of 517

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Select item 14899792221.

rs1489979222 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:58646097 (GRCh38)
15:58938296 (GRCh37)
Canonical SPDI:: NC_000015.10:58646096:C:A
Gene:: ADAM10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.58646097C>A, NC_000015.9:g.58938296C>A, NG_033876.2:g.108611G>T, NM_001110.4:c.693G>T, NM_001110.3:c.693G>T, NM_001110.2:c.693G>T, NM_001320570.2:c.693G>T, NM_001320570.1:c.693G>T, NP_001101.1:p.Leu231Phe, NP_001307499.1:p.Leu231Phe

Select item 14894981902.

rs1489498190 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:58643919 (GRCh38)
15:58936118 (GRCh37)
Canonical SPDI:: NC_000015.10:58643918:G:T
Gene:: ADAM10 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.58643919G>T, NC_000015.9:g.58936118G>T, NG_033876.2:g.110789C>A, NM_001110.4:c.795C>A, NM_001110.3:c.795C>A, NM_001110.2:c.795C>A

Select item 14893952093.

rs1489395209 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 15:58679240 (GRCh38)
15:58971439 (GRCh37)
Canonical SPDI:: NC_000015.10:58679239:C:A,NC_000015.10:58679239:C:G,NC_000015.10:58679239:C:T
Gene:: ADAM10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.58679240C>A, NC_000015.10:g.58679240C>G, NC_000015.10:g.58679240C>T, NC_000015.9:g.58971439C>A, NC_000015.9:g.58971439C>G, NC_000015.9:g.58971439C>T, NG_033876.2:g.75468G>T, NG_033876.2:g.75468G>C, NG_033876.2:g.75468G>A, NM_001110.4:c.368G>T, NM_001110.4:c.368G>C, NM_001110.4:c.368G>A, NM_001110.3:c.368G>T, NM_001110.3:c.368G>C, NM_001110.3:c.368G>A, NM_001110.2:c.368G>T, NM_001110.2:c.368G>C, NM_001110.2:c.368G>A, NM_001320570.2:c.368G>T, NM_001320570.2:c.368G>C, NM_001320570.2:c.368G>A, NM_001320570.1:c.368G>T, NM_001320570.1:c.368G>C, NM_001320570.1:c.368G>A, NP_001101.1:p.Arg123Ile, NP_001101.1:p.Arg123Thr, NP_001101.1:p.Arg123Lys, NP_001307499.1:p.Arg123Ile, NP_001307499.1:p.Arg123Thr, NP_001307499.1:p.Arg123Lys

Select item 14882338594.

rs1488233859 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:58611990 (GRCh38)
15:58904189 (GRCh37)
Canonical SPDI:: NC_000015.10:58611989:G:T
Gene:: ADAM10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.58611990G>T, NC_000015.9:g.58904189G>T, NG_033876.2:g.142718C>A, NM_001110.4:c.1513C>A, NM_001110.3:c.1513C>A, NM_001110.2:c.1513C>A, NM_001320570.2:c.1420C>A, NM_001320570.1:c.1420C>A, NP_001101.1:p.Pro505Thr, NP_001307499.1:p.Pro474Thr

Select item 14849094585.

rs1484909458 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:58640845 (GRCh38)
15:58933044 (GRCh37)
Canonical SPDI:: NC_000015.10:58640844:G:A
Gene:: ADAM10 (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_000015.10:g.58640845G>A, NC_000015.9:g.58933044G>A, NG_033876.2:g.113863C>T, NM_001110.4:c.944C>T, NM_001110.3:c.944C>T, NM_001110.2:c.944C>T, NM_001320570.2:c.851C>T, NM_001320570.1:c.851C>T, NP_001101.1:p.Ala315Val, NP_001307499.1:p.Ala284Val

Select item 14829286526.

rs1482928652 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:58633241 (GRCh38)
15:58925440 (GRCh37)
Canonical SPDI:: NC_000015.10:58633240:A:G
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.58633241A>G, NC_000015.9:g.58925440A>G, NG_033876.2:g.121467T>C, NM_001110.4:c.1131T>C, NM_001110.3:c.1131T>C, NM_001110.2:c.1131T>C, NM_001320570.2:c.1038T>C, NM_001320570.1:c.1038T>C

Select item 14819533627.

rs1481953362 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:58643939 (GRCh38)
15:58936138 (GRCh37)
Canonical SPDI:: NC_000015.10:58643938:T:C
Gene:: ADAM10 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.58643939T>C, NC_000015.9:g.58936138T>C, NG_033876.2:g.110769A>G, NM_001110.4:c.775A>G, NM_001110.3:c.775A>G, NM_001110.2:c.775A>G, NP_001101.1:p.Thr259Ala

Select item 14794748588.

rs1479474858 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:58682292 (GRCh38)
15:58974491 (GRCh37)
Canonical SPDI:: NC_000015.10:58682291:T:C
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.58682292T>C, NC_000015.9:g.58974491T>C, NG_033876.2:g.72416A>G, NM_001110.4:c.229A>G, NM_001110.3:c.229A>G, NM_001110.2:c.229A>G, NM_001320570.2:c.229A>G, NM_001320570.1:c.229A>G, NP_001101.1:p.Arg77Gly, NP_001307499.1:p.Arg77Gly

Select item 14773416959.

rs1477341695 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:58610496 (GRCh38)
15:58902695 (GRCh37)
Canonical SPDI:: NC_000015.10:58610495:C:G
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.58610496C>G, NC_000015.9:g.58902695C>G, NG_033876.2:g.144212G>C, NM_001110.4:c.1826G>C, NM_001110.3:c.1826G>C, NM_001110.2:c.1826G>C, NM_001320570.2:c.1733G>C, NM_001320570.1:c.1733G>C, NP_001101.1:p.Ser609Thr, NP_001307499.1:p.Ser578Thr

Select item 147639601510.

rs1476396015 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:58611080 (GRCh38)
15:58903279 (GRCh37)
Canonical SPDI:: NC_000015.10:58611079:A:G
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000015/4 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000015.10:g.58611080A>G, NC_000015.9:g.58903279A>G, NG_033876.2:g.143628T>C, NM_001110.4:c.1723T>C, NM_001110.3:c.1723T>C, NM_001110.2:c.1723T>C, NM_001320570.2:c.1630T>C, NM_001320570.1:c.1630T>C, NP_001101.1:p.Tyr575His, NP_001307499.1:p.Tyr544His

Select item 147480914511.

rs1474809145 [Homo sapiens]

Variant type:: INS
Alleles:: ->CTA [Show Flanks]
Chromosome:: 15:58717704 (GRCh38)
15:59009904 (GRCh37)
Canonical SPDI:: NC_000015.10:58717704::CTA
Gene:: ADAM10 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
HGVS:: NC_000015.10:g.58717704_58717705insCTA, NC_000015.9:g.59009903_59009904insCTA, NG_033876.2:g.37003_37004insTAG, NM_001110.4:c.78_79insTAG, NM_001110.3:c.78_79insTAG, NM_001110.2:c.78_79insTAG, NM_001320570.2:c.78_79insTAG, NM_001320570.1:c.78_79insTAG, NP_001101.1:p.Lys27Ter, NP_001307499.1:p.Lys27Ter

Select item 147425665312.

rs1474256653 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:58610362 (GRCh38)
15:58902561 (GRCh37)
Canonical SPDI:: NC_000015.10:58610361:G:A
Gene:: ADAM10 (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_000015.10:g.58610362G>A, NC_000015.9:g.58902561G>A, NG_033876.2:g.144346C>T, NM_001110.4:c.1960C>T, NM_001110.3:c.1960C>T, NM_001110.2:c.1960C>T, NM_001320570.2:c.1867C>T, NM_001320570.1:c.1867C>T

Select item 147269574813.

rs1472695748 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:58640838 (GRCh38)
15:58933037 (GRCh37)
Canonical SPDI:: NC_000015.10:58640837:G:A
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.58640838G>A, NC_000015.9:g.58933037G>A, NG_033876.2:g.113870C>T, NM_001110.4:c.951C>T, NM_001110.3:c.951C>T, NM_001110.2:c.951C>T, NM_001320570.2:c.858C>T, NM_001320570.1:c.858C>T

Select item 147260166014.

rs1472601660 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:58682219 (GRCh38)
15:58974418 (GRCh37)
Canonical SPDI:: NC_000015.10:58682218:T:C
Gene:: ADAM10 (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_000015.10:g.58682219T>C, NC_000015.9:g.58974418T>C, NG_033876.2:g.72489A>G, NM_001110.4:c.302A>G, NM_001110.3:c.302A>G, NM_001110.2:c.302A>G, NM_001320570.2:c.302A>G, NM_001320570.1:c.302A>G, NP_001101.1:p.His101Arg, NP_001307499.1:p.His101Arg

Select item 147237586715.

rs1472375867 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:58627818 (GRCh38)
15:58920017 (GRCh37)
Canonical SPDI:: NC_000015.10:58627817:A:G
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000054/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000015.10:g.58627818A>G, NC_000015.9:g.58920017A>G, NG_033876.2:g.126890T>C, NM_001110.4:c.1242T>C, NM_001110.3:c.1242T>C, NM_001110.2:c.1242T>C, NM_001320570.2:c.1149T>C, NM_001320570.1:c.1149T>C

Select item 147228452916.

rs1472284529 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:58646116 (GRCh38)
15:58938315 (GRCh37)
Canonical SPDI:: NC_000015.10:58646115:T:C
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.58646116T>C, NC_000015.9:g.58938315T>C, NG_033876.2:g.108592A>G, NM_001110.4:c.674A>G, NM_001110.3:c.674A>G, NM_001110.2:c.674A>G, NM_001320570.2:c.674A>G, NM_001320570.1:c.674A>G, NP_001101.1:p.Tyr225Cys, NP_001307499.1:p.Tyr225Cys

Select item 146863812117.

rs1468638121 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:58717588 (GRCh38)
15:59009787 (GRCh37)
Canonical SPDI:: NC_000015.10:58717587:A:G
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000342/1 (KOREAN)
HGVS:: NC_000015.10:g.58717588A>G, NC_000015.9:g.59009787A>G, NG_033876.2:g.37120T>C, NM_001110.4:c.195T>C, NM_001110.3:c.195T>C, NM_001110.2:c.195T>C, NM_001320570.2:c.195T>C, NM_001320570.1:c.195T>C

Select item 146858634218.

rs1468586342 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:58627761 (GRCh38)
15:58919960 (GRCh37)
Canonical SPDI:: NC_000015.10:58627760:T:C
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000015.10:g.58627761T>C, NC_000015.9:g.58919960T>C, NG_033876.2:g.126947A>G, NM_001110.4:c.1299A>G, NM_001110.3:c.1299A>G, NM_001110.2:c.1299A>G, NM_001320570.2:c.1206A>G, NM_001320570.1:c.1206A>G

Select item 146849502919.

rs1468495029 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:58610473 (GRCh38)
15:58902672 (GRCh37)
Canonical SPDI:: NC_000015.10:58610472:T:G
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.58610473T>G, NC_000015.9:g.58902672T>G, NG_033876.2:g.144235A>C, NM_001110.4:c.1849A>C, NM_001110.3:c.1849A>C, NM_001110.2:c.1849A>C, NM_001320570.2:c.1756A>C, NM_001320570.1:c.1756A>C

Select item 146781348220.

rs1467813482 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:58679277 (GRCh38)
15:58971476 (GRCh37)
Canonical SPDI:: NC_000015.10:58679276:C:G,NC_000015.10:58679276:C:T
Gene:: ADAM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000015.10:g.58679277C>G, NC_000015.10:g.58679277C>T, NC_000015.9:g.58971476C>G, NC_000015.9:g.58971476C>T, NG_033876.2:g.75431G>C, NG_033876.2:g.75431G>A, NM_001110.4:c.331G>C, NM_001110.4:c.331G>A, NM_001110.3:c.331G>C, NM_001110.3:c.331G>A, NM_001110.2:c.331G>C, NM_001110.2:c.331G>A, NM_001320570.2:c.331G>C, NM_001320570.2:c.331G>A, NM_001320570.1:c.331G>C, NM_001320570.1:c.331G>A, NP_001101.1:p.Glu111Gln, NP_001101.1:p.Glu111Lys, NP_001307499.1:p.Glu111Gln, NP_001307499.1:p.Glu111Lys

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