SNP Links for Protein (Select 767960197) - SNP

Links from Protein

Items: 1 to 20 of 882

<< First< Prev

Page of 45

Next >Last >>

Select item 14909844411.

rs1490984441 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:13195118 (GRCh38)
10:13237118 (GRCh37)
Canonical SPDI:: NC_000010.11:13195117:G:A,NC_000010.11:13195117:G:C
Gene:: MCM10 (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)
A=0.000342/1 (KOREAN)
HGVS:: NC_000010.11:g.13195118G>A, NC_000010.11:g.13195118G>C, NC_000010.10:g.13237118G>A, NC_000010.10:g.13237118G>C, NM_018518.5:c.1823G>A, NM_018518.5:c.1823G>C, NM_018518.4:c.1823G>A, NM_018518.4:c.1823G>C, XM_011519538.3:c.1826G>A, XM_011519538.3:c.1826G>C, XM_011519538.2:c.1826G>A, XM_011519538.2:c.1826G>C, XM_011519538.1:c.1826G>A, XM_011519538.1:c.1826G>C, NM_182751.3:c.1826G>A, NM_182751.3:c.1826G>C, NM_182751.2:c.1826G>A, NM_182751.2:c.1826G>C, XM_047425437.1:c.1823G>A, XM_047425437.1:c.1823G>C, NP_060988.3:p.Arg608Gln, NP_060988.3:p.Arg608Pro, XP_011517840.1:p.Arg609Gln, XP_011517840.1:p.Arg609Pro, NP_877428.1:p.Arg609Gln, NP_877428.1:p.Arg609Pro, XP_047281393.1:p.Arg608Gln, XP_047281393.1:p.Arg608Pro

Select item 14901013262.

rs1490101326 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:13195076 (GRCh38)
10:13237076 (GRCh37)
Canonical SPDI:: NC_000010.11:13195075:C:A
Gene:: MCM10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000010.11:g.13195076C>A, NC_000010.10:g.13237076C>A, NM_018518.5:c.1781C>A, NM_018518.4:c.1781C>A, XM_011519538.3:c.1784C>A, XM_011519538.2:c.1784C>A, XM_011519538.1:c.1784C>A, NM_182751.3:c.1784C>A, NM_182751.2:c.1784C>A, XM_047425437.1:c.1781C>A, NP_060988.3:p.Ala594Asp, XP_011517840.1:p.Ala595Asp, NP_877428.1:p.Ala595Asp, XP_047281393.1:p.Ala594Asp

Select item 14848892183.

rs1484889218 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:13172377 (GRCh38)
10:13214377 (GRCh37)
Canonical SPDI:: NC_000010.11:13172376:G:T
Gene:: MCM10 (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=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000010.11:g.13172377G>T, NC_000010.10:g.13214377G>T, NM_018518.5:c.351G>T, NM_018518.4:c.351G>T, XM_011519538.3:c.351G>T, XM_011519538.2:c.351G>T, XM_011519538.1:c.351G>T, NM_182751.3:c.351G>T, NM_182751.2:c.351G>T, XM_047425437.1:c.351G>T, NP_060988.3:p.Glu117Asp, XP_011517840.1:p.Glu117Asp, NP_877428.1:p.Glu117Asp, XP_047281393.1:p.Glu117Asp

Select item 14838775674.

rs1483877567 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:13197682 (GRCh38)
10:13239682 (GRCh37)
Canonical SPDI:: NC_000010.11:13197681:C:G,NC_000010.11:13197681:C:T
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.13197682C>G, NC_000010.11:g.13197682C>T, NC_000010.10:g.13239682C>G, NC_000010.10:g.13239682C>T, NM_018518.5:c.2034C>G, NM_018518.5:c.2034C>T, NM_018518.4:c.2034C>G, NM_018518.4:c.2034C>T, XM_011519538.3:c.2037C>G, XM_011519538.3:c.2037C>T, XM_011519538.2:c.2037C>G, XM_011519538.2:c.2037C>T, XM_011519538.1:c.2037C>G, XM_011519538.1:c.2037C>T, NM_182751.3:c.2037C>G, NM_182751.3:c.2037C>T, NM_182751.2:c.2037C>G, NM_182751.2:c.2037C>T, XM_047425437.1:c.2034C>G, XM_047425437.1:c.2034C>T, NP_060988.3:p.Asn678Lys, XP_011517840.1:p.Asn679Lys, NP_877428.1:p.Asn679Lys, XP_047281393.1:p.Asn678Lys

Select item 14838630295.

rs1483863029 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:13175650 (GRCh38)
10:13217650 (GRCh37)
Canonical SPDI:: NC_000010.11:13175649:T:C
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000010.11:g.13175650T>C, NC_000010.10:g.13217650T>C, NM_018518.5:c.733T>C, NM_018518.4:c.733T>C, XM_011519538.3:c.736T>C, XM_011519538.2:c.736T>C, XM_011519538.1:c.736T>C, NM_182751.3:c.736T>C, NM_182751.2:c.736T>C, XM_047425437.1:c.733T>C, NP_060988.3:p.Cys245Arg, XP_011517840.1:p.Cys246Arg, NP_877428.1:p.Cys246Arg, XP_047281393.1:p.Cys245Arg

Select item 14837544246.

rs1483754424 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:13201439 (GRCh38)
10:13243439 (GRCh37)
Canonical SPDI:: NC_000010.11:13201438:G:T
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.13201439G>T, NC_000010.10:g.13243439G>T, NM_018518.5:c.2257G>T, NM_018518.4:c.2257G>T, XM_011519538.3:c.2260G>T, XM_011519538.2:c.2260G>T, XM_011519538.1:c.2260G>T, NM_182751.3:c.2260G>T, NM_182751.2:c.2260G>T, XM_047425437.1:c.2257G>T, NP_060988.3:p.Glu753Ter, XP_011517840.1:p.Glu754Ter, NP_877428.1:p.Glu754Ter, XP_047281393.1:p.Glu753Ter

Select item 14833380057.

rs1483338005 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 10:13183100 (GRCh38)
10:13225100 (GRCh37)
Canonical SPDI:: NC_000010.11:13183099:GG:G
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,splice_donor_variant
Validated:: by frequency,by alfa
MAF:: GG=0.000111/1 (ALFA)
-=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.13183101del, NC_000010.10:g.13225101del

Select item 14801178988.

rs1480117898 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:13171081 (GRCh38)
10:13213081 (GRCh37)
Canonical SPDI:: NC_000010.11:13171080:C:G
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.13171081C>G, NC_000010.10:g.13213081C>G, NM_018518.5:c.167C>G, NM_018518.4:c.167C>G, XM_011519538.3:c.167C>G, XM_011519538.2:c.167C>G, XM_011519538.1:c.167C>G, NM_182751.3:c.167C>G, NM_182751.2:c.167C>G, XM_047425437.1:c.167C>G, NP_060988.3:p.Thr56Arg, XP_011517840.1:p.Thr56Arg, NP_877428.1:p.Thr56Arg, XP_047281393.1:p.Thr56Arg

Select item 14792763209.

rs1479276320 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:13198791 (GRCh38)
10:13240791 (GRCh37)
Canonical SPDI:: NC_000010.11:13198785:ACACACA:ACACA
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.13198787CA[2], NC_000010.10:g.13240787CA[2], NM_018518.5:c.2222_2223del, NM_018518.4:c.2222_2223del, XM_011519538.3:c.2225_2226del, XM_011519538.2:c.2225_2226del, XM_011519538.1:c.2225_2226del, NM_182751.3:c.2225_2226del, NM_182751.2:c.2225_2226del, XM_047425437.1:c.2222_2223del, NP_060988.3:p.Thr741fs, XP_011517840.1:p.Thr742fs, NP_877428.1:p.Thr742fs, XP_047281393.1:p.Thr741fs

Select item 147922618210.

rs1479226182 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:13209258 (GRCh38)
10:13251258 (GRCh37)
Canonical SPDI:: NC_000010.11:13209257:C:T
Gene:: MCM10 (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=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.13209258C>T, NC_000010.10:g.13251258C>T, NM_018518.5:c.2573C>T, NM_018518.4:c.2573C>T, XM_011519538.3:c.2576C>T, XM_011519538.2:c.2576C>T, XM_011519538.1:c.2576C>T, NM_182751.3:c.2576C>T, NM_182751.2:c.2576C>T, XM_047425437.1:c.2573C>T, NP_060988.3:p.Thr858Ile, XP_011517840.1:p.Thr859Ile, NP_877428.1:p.Thr859Ile, XP_047281393.1:p.Thr858Ile

Select item 147851163411.

rs1478511634 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:13171233 (GRCh38)
10:13213233 (GRCh37)
Canonical SPDI:: NC_000010.11:13171232:A:G
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.13171233A>G, NC_000010.10:g.13213233A>G, NM_018518.5:c.319A>G, NM_018518.4:c.319A>G, XM_011519538.3:c.319A>G, XM_011519538.2:c.319A>G, XM_011519538.1:c.319A>G, NM_182751.3:c.319A>G, NM_182751.2:c.319A>G, XM_047425437.1:c.319A>G, NP_060988.3:p.Arg107Gly, XP_011517840.1:p.Arg107Gly, NP_877428.1:p.Arg107Gly, XP_047281393.1:p.Arg107Gly

Select item 147748771112.

rs1477487711 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:13192318 (GRCh38)
10:13234318 (GRCh37)
Canonical SPDI:: NC_000010.11:13192317:G:A
Gene:: MCM10 (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)
HGVS:: NC_000010.11:g.13192318G>A, NC_000010.10:g.13234318G>A, NM_018518.5:c.1580G>A, NM_018518.4:c.1580G>A, XM_011519538.3:c.1583G>A, XM_011519538.2:c.1583G>A, XM_011519538.1:c.1583G>A, NM_182751.3:c.1583G>A, NM_182751.2:c.1583G>A, XM_047425437.1:c.1580G>A, NP_060988.3:p.Cys527Tyr, XP_011517840.1:p.Cys528Tyr, NP_877428.1:p.Cys528Tyr, XP_047281393.1:p.Cys527Tyr

Select item 147578294213.

rs1475782942 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAGAGAACAACTTG>- [Show Flanks]
Chromosome:: 10:13198723 (GRCh38)
10:13240723 (GRCh37)
Canonical SPDI:: NC_000010.11:13198721:GGAGAGAACAACTTG:G
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.13198723_13198736del, NC_000010.10:g.13240723_13240736del, NM_018518.5:c.2154_2167del, NM_018518.4:c.2154_2167del, XM_011519538.3:c.2157_2170del, XM_011519538.2:c.2157_2170del, XM_011519538.1:c.2157_2170del, NM_182751.3:c.2157_2170del, NM_182751.2:c.2157_2170del, XM_047425437.1:c.2154_2167del, NP_060988.3:p.Arg718fs, XP_011517840.1:p.Arg719fs, NP_877428.1:p.Arg719fs, XP_047281393.1:p.Arg718fs

Select item 147534303114.

rs1475343031 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:13171256 (GRCh38)
10:13213256 (GRCh37)
Canonical SPDI:: NC_000010.11:13171255:G:A
Gene:: MCM10 (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=0.000012/3 (GnomAD_exomes)
A=0.000142/2 (TOMMO)
HGVS:: NC_000010.11:g.13171256G>A, NC_000010.10:g.13213256G>A, NM_018518.5:c.342G>A, NM_018518.4:c.342G>A, XM_011519538.3:c.342G>A, XM_011519538.2:c.342G>A, XM_011519538.1:c.342G>A, NM_182751.3:c.342G>A, NM_182751.2:c.342G>A, XM_047425437.1:c.342G>A

Select item 147430241115.

rs1474302411 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:13172631 (GRCh38)
10:13214631 (GRCh37)
Canonical SPDI:: NC_000010.11:13172630:A:G
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000047/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.13172631A>G, NC_000010.10:g.13214631A>G, NM_018518.5:c.458A>G, NM_018518.4:c.458A>G, XM_011519538.3:c.461A>G, XM_011519538.2:c.461A>G, XM_011519538.1:c.461A>G, NM_182751.3:c.461A>G, NM_182751.2:c.461A>G, XM_047425437.1:c.458A>G, NP_060988.3:p.Lys153Arg, XP_011517840.1:p.Lys154Arg, NP_877428.1:p.Lys154Arg, XP_047281393.1:p.Lys153Arg

Select item 147114954016.

rs1471149540 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:13170926 (GRCh38)
10:13212926 (GRCh37)
Canonical SPDI:: NC_000010.11:13170925:G:A
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.13170926G>A, NC_000010.10:g.13212926G>A, NM_018518.5:c.12G>A, NM_018518.4:c.12G>A, XM_011519538.3:c.12G>A, XM_011519538.2:c.12G>A, XM_011519538.1:c.12G>A, NM_182751.3:c.12G>A, NM_182751.2:c.12G>A, XM_047425437.1:c.12G>A

Select item 146673836717.

rs1466738367 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:13175655 (GRCh38)
10:13217655 (GRCh37)
Canonical SPDI:: NC_000010.11:13175654:G:A
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0.000047/1 (ALFA)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.13175655G>A, NC_000010.10:g.13217655G>A, NM_018518.5:c.738G>A, NM_018518.4:c.738G>A, XM_011519538.3:c.741G>A, XM_011519538.2:c.741G>A, XM_011519538.1:c.741G>A, NM_182751.3:c.741G>A, NM_182751.2:c.741G>A, XM_047425437.1:c.738G>A

Select item 146656084418.

rs1466560844 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:13188901 (GRCh38)
10:13230901 (GRCh37)
Canonical SPDI:: NC_000010.11:13188900:G:A
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.13188901G>A, NC_000010.10:g.13230901G>A, NM_018518.5:c.1236G>A, NM_018518.4:c.1236G>A, XM_011519538.3:c.1239G>A, XM_011519538.2:c.1239G>A, XM_011519538.1:c.1239G>A, NM_182751.3:c.1239G>A, NM_182751.2:c.1239G>A, XM_047425437.1:c.1236G>A

Select item 146572265819.

rs1465722658 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:13201467 (GRCh38)
10:13243467 (GRCh37)
Canonical SPDI:: NC_000010.11:13201466:A:G
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000010.11:g.13201467A>G, NC_000010.10:g.13243467A>G, NM_018518.5:c.2285A>G, NM_018518.4:c.2285A>G, XM_011519538.3:c.2288A>G, XM_011519538.2:c.2288A>G, XM_011519538.1:c.2288A>G, NM_182751.3:c.2288A>G, NM_182751.2:c.2288A>G, XM_047425437.1:c.2285A>G, NP_060988.3:p.Lys762Arg, XP_011517840.1:p.Lys763Arg, NP_877428.1:p.Lys763Arg, XP_047281393.1:p.Lys762Arg

Select item 146460970820.

rs1464609708 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:13170947 (GRCh38)
10:13212947 (GRCh37)
Canonical SPDI:: NC_000010.11:13170946:G:A
Gene:: MCM10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.13170947G>A, NC_000010.10:g.13212947G>A, NM_018518.5:c.33G>A, NM_018518.4:c.33G>A, XM_011519538.3:c.33G>A, XM_011519538.2:c.33G>A, XM_011519538.1:c.33G>A, NM_182751.3:c.33G>A, NM_182751.2:c.33G>A, XM_047425437.1:c.33G>A

<< First< Prev

Page of 45

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 882

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity