SNP Links for Protein (Select 1034675523) - SNP

Links from Protein

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Select item 14863694551.

rs1486369455 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:50346732 (GRCh38)
X:50089731 (GRCh37)
Canonical SPDI:: NC_000023.11:50346731:A:G
Gene:: CCNB3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.50346732A>G, NW_004070877.1:g.59847A>G, NG_012880.1:g.65558A>G, NM_033670.4:c.423A>G, NM_033670.3:c.423A>G, NM_033670.2:c.423A>G, NM_033031.3:c.3735A>G, NM_033031.2:c.3735A>G, NC_000023.10:g.50089731A>G, XM_017029914.2:c.3762A>G, XM_017029914.1:c.3762A>G, XM_024452472.2:c.3762A>G, XM_024452472.1:c.3762A>G, XM_017029913.1:c.3762A>G, XM_017029916.1:c.3759A>G, XM_017029917.1:c.3738A>G, XM_017029915.1:c.3762A>G, XM_047442599.1:c.3738A>G, XM_047442600.1:c.3735A>G, NM_033671.1:c.*407A>G

Select item 14860394392.

rs1486039439 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:50310580 (GRCh38)
X:50053580 (GRCh37)
Canonical SPDI:: NC_000023.11:50310579:T:C
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.50310580T>C, NW_004070877.1:g.23695T>C, NG_012880.1:g.29407T>C, NM_033031.3:c.2411T>C, NM_033031.2:c.2411T>C, NC_000023.10:g.50053580T>C, XM_017029914.2:c.2411T>C, XM_017029914.1:c.2411T>C, XM_024452472.2:c.2411T>C, XM_024452472.1:c.2411T>C, XM_017029913.1:c.2411T>C, XM_017029916.1:c.2411T>C, XM_017029917.1:c.2411T>C, XM_017029915.1:c.2411T>C, XM_047442599.1:c.2411T>C, XM_047442600.1:c.2411T>C, NP_149020.2:p.Met804Thr, XP_016885403.1:p.Met804Thr, XP_024308240.1:p.Met804Thr, XP_016885402.1:p.Met804Thr, XP_016885405.1:p.Met804Thr, XP_016885406.1:p.Met804Thr, XP_016885404.1:p.Met804Thr, XP_047298555.1:p.Met804Thr, XP_047298556.1:p.Met804Thr

Select item 14840449203.

rs1484044920 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:50309901 (GRCh38)
X:50052901 (GRCh37)
Canonical SPDI:: NC_000023.11:50309900:G:C
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.50309901G>C, NW_004070877.1:g.23016G>C, NG_012880.1:g.28728G>C, NM_033031.3:c.1732G>C, NM_033031.2:c.1732G>C, NC_000023.10:g.50052901G>C, XM_017029914.2:c.1732G>C, XM_017029914.1:c.1732G>C, XM_024452472.2:c.1732G>C, XM_024452472.1:c.1732G>C, XM_017029913.1:c.1732G>C, XM_017029916.1:c.1732G>C, XM_017029917.1:c.1732G>C, XM_017029915.1:c.1732G>C, XM_047442599.1:c.1732G>C, XM_047442600.1:c.1732G>C, NP_149020.2:p.Glu578Gln, XP_016885403.1:p.Glu578Gln, XP_024308240.1:p.Glu578Gln, XP_016885402.1:p.Glu578Gln, XP_016885405.1:p.Glu578Gln, XP_016885406.1:p.Glu578Gln, XP_016885404.1:p.Glu578Gln, XP_047298555.1:p.Glu578Gln, XP_047298556.1:p.Glu578Gln

Select item 14833101584.

rs1483310158 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:50288830 (GRCh38)
X:50031830 (GRCh37)
Canonical SPDI:: NC_000023.11:50288829:T:C
Gene:: CCNB3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000006/1 (GnomAD_exomes)
C=0.00001/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.50288830T>C, NW_004070877.1:g.1945T>C, NG_012880.1:g.7657T>C, NM_033670.4:c.147T>C, NM_033670.3:c.147T>C, NM_033670.2:c.147T>C, NM_033031.3:c.147T>C, NM_033031.2:c.147T>C, NW_021160028.1:g.28769T>C, NC_000023.10:g.50031830T>C, XM_017029914.2:c.147T>C, XM_017029914.1:c.147T>C, XM_024452472.2:c.147T>C, XM_024452472.1:c.147T>C, XM_017029913.1:c.147T>C, XM_017029916.1:c.147T>C, XM_017029917.1:c.147T>C, XM_017029915.1:c.147T>C, XM_047442599.1:c.147T>C, NM_033671.1:c.147T>C, XM_047442600.1:c.147T>C

Select item 14817512035.

rs1481751203 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:50310867 (GRCh38)
X:50053867 (GRCh37)
Canonical SPDI:: NC_000023.11:50310866:G:A
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.50310867G>A, NW_004070877.1:g.23982G>A, NG_012880.1:g.29694G>A, NM_033031.3:c.2698G>A, NM_033031.2:c.2698G>A, NC_000023.10:g.50053867G>A, XM_017029914.2:c.2698G>A, XM_017029914.1:c.2698G>A, XM_024452472.2:c.2698G>A, XM_024452472.1:c.2698G>A, XM_017029913.1:c.2698G>A, XM_017029916.1:c.2698G>A, XM_017029917.1:c.2698G>A, XM_017029915.1:c.2698G>A, XM_047442599.1:c.2698G>A, XM_047442600.1:c.2698G>A, NP_149020.2:p.Glu900Lys, XP_016885403.1:p.Glu900Lys, XP_024308240.1:p.Glu900Lys, XP_016885402.1:p.Glu900Lys, XP_016885405.1:p.Glu900Lys, XP_016885406.1:p.Glu900Lys, XP_016885404.1:p.Glu900Lys, XP_047298555.1:p.Glu900Lys, XP_047298556.1:p.Glu900Lys

Select item 14781689736.

rs1478168973 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:50351338 (GRCh38)
X:50094337 (GRCh37)
Canonical SPDI:: NC_000023.11:50351337:G:A
Gene:: CCNB3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000005/1 (GnomAD_exomes)
A=0.000026/7 (TOPMED)
A=0.000045/1 (TOMMO)
HGVS:: NC_000023.11:g.50351338G>A, NW_004070877.1:g.64453G>A, NG_012880.1:g.70164G>A, NM_033670.4:c.746G>A, NM_033670.3:c.746G>A, NM_033670.2:c.746G>A, NM_033031.3:c.4058G>A, NM_033031.2:c.4058G>A, NC_000023.10:g.50094337G>A, XM_017029914.2:c.4085G>A, XM_017029914.1:c.4085G>A, XM_024452472.2:c.4085G>A, XM_024452472.1:c.4085G>A, XM_017029913.1:c.4085G>A, XM_017029916.1:c.4082G>A, XM_017029917.1:c.4061G>A, XM_017029915.1:c.4085G>A, XM_047442599.1:c.4061G>A, XM_047442600.1:c.4058G>A, NM_033671.1:c.*730G>A, NP_391990.1:p.Ser249Asn, NP_149020.2:p.Ser1353Asn, XP_016885403.1:p.Ser1362Asn, XP_024308240.1:p.Ser1362Asn, XP_016885402.1:p.Ser1362Asn, XP_016885405.1:p.Ser1361Asn, XP_016885406.1:p.Ser1354Asn, XP_016885404.1:p.Ser1362Asn, XP_047298555.1:p.Ser1354Asn, XP_047298556.1:p.Ser1353Asn

Select item 14652082787.

rs1465208278 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:50308575 (GRCh38)
X:50051575 (GRCh37)
Canonical SPDI:: NC_000023.11:50308574:A:G
Gene:: CCNB3 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00003/8 (TOPMED)
G=0.000048/5 (GnomAD)
HGVS:: NC_000023.11:g.50308575A>G, NW_004070877.1:g.21690A>G, NG_012880.1:g.27402A>G, NM_033031.3:c.406A>G, NM_033031.2:c.406A>G, NC_000023.10:g.50051575A>G, XM_017029914.2:c.406A>G, XM_017029914.1:c.406A>G, XM_024452472.2:c.406A>G, XM_024452472.1:c.406A>G, XM_017029913.1:c.406A>G, XM_017029916.1:c.406A>G, XM_017029917.1:c.406A>G, XM_017029915.1:c.406A>G, XM_047442599.1:c.406A>G, XM_047442600.1:c.406A>G, NP_149020.2:p.Ile136Val, XP_016885403.1:p.Ile136Val, XP_024308240.1:p.Ile136Val, XP_016885402.1:p.Ile136Val, XP_016885405.1:p.Ile136Val, XP_016885406.1:p.Ile136Val, XP_016885404.1:p.Ile136Val, XP_047298555.1:p.Ile136Val, XP_047298556.1:p.Ile136Val

Select item 14579886438.

rs1457988643 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:50309638 (GRCh38)
X:50052638 (GRCh37)
Canonical SPDI:: NC_000023.11:50309637:T:A
Gene:: CCNB3 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.50309638T>A, NW_004070877.1:g.22753T>A, NG_012880.1:g.28465T>A, NM_033031.3:c.1469T>A, NM_033031.2:c.1469T>A, NC_000023.10:g.50052638T>A, XM_017029914.2:c.1469T>A, XM_017029914.1:c.1469T>A, XM_024452472.2:c.1469T>A, XM_024452472.1:c.1469T>A, XM_017029913.1:c.1469T>A, XM_017029916.1:c.1469T>A, XM_017029917.1:c.1469T>A, XM_017029915.1:c.1469T>A, XM_047442599.1:c.1469T>A, XM_047442600.1:c.1469T>A, NP_149020.2:p.Ile490Asn, XP_016885403.1:p.Ile490Asn, XP_024308240.1:p.Ile490Asn, XP_016885402.1:p.Ile490Asn, XP_016885405.1:p.Ile490Asn, XP_016885406.1:p.Ile490Asn, XP_016885404.1:p.Ile490Asn, XP_047298555.1:p.Ile490Asn, XP_047298556.1:p.Ile490Asn

Select item 14554683989.

rs1455468398 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:50309406 (GRCh38)
X:50052406 (GRCh37)
Canonical SPDI:: NC_000023.11:50309405:C:T
Gene:: CCNB3 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.50309406C>T, NW_004070877.1:g.22521C>T, NG_012880.1:g.28233C>T, NM_033031.3:c.1237C>T, NM_033031.2:c.1237C>T, NC_000023.10:g.50052406C>T, XM_017029914.2:c.1237C>T, XM_017029914.1:c.1237C>T, XM_024452472.2:c.1237C>T, XM_024452472.1:c.1237C>T, XM_017029913.1:c.1237C>T, XM_017029916.1:c.1237C>T, XM_017029917.1:c.1237C>T, XM_017029915.1:c.1237C>T, XM_047442599.1:c.1237C>T, XM_047442600.1:c.1237C>T, NP_149020.2:p.Leu413Phe, XP_016885403.1:p.Leu413Phe, XP_024308240.1:p.Leu413Phe, XP_016885402.1:p.Leu413Phe, XP_016885405.1:p.Leu413Phe, XP_016885406.1:p.Leu413Phe, XP_016885404.1:p.Leu413Phe, XP_047298555.1:p.Leu413Phe, XP_047298556.1:p.Leu413Phe

Select item 145431534310.

rs1454315343 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:50312867 (GRCh38)
X:50055867 (GRCh37)
Canonical SPDI:: NC_000023.11:50312866:A:G
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.50312867A>G, NW_004070877.1:g.25982A>G, NG_012880.1:g.31694A>G, NC_000023.10:g.50055867A>G, XM_017029914.2:c.3427A>G, XM_017029914.1:c.3427A>G, XM_024452472.2:c.3427A>G, XM_024452472.1:c.3427A>G, XM_017029913.1:c.3427A>G, XM_017029916.1:c.3424A>G, XM_017029915.1:c.3427A>G, XP_016885403.1:p.Ile1143Val, XP_024308240.1:p.Ile1143Val, XP_016885402.1:p.Ile1143Val, XP_016885405.1:p.Ile1142Val, XP_016885404.1:p.Ile1143Val

Select item 145322133811.

rs1453221338 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:50310629 (GRCh38)
X:50053629 (GRCh37)
Canonical SPDI:: NC_000023.11:50310628:T:A
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000008/2 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.50310629T>A, NW_004070877.1:g.23744T>A, NG_012880.1:g.29456T>A, NM_033031.3:c.2460T>A, NM_033031.2:c.2460T>A, NC_000023.10:g.50053629T>A, XM_017029914.2:c.2460T>A, XM_017029914.1:c.2460T>A, XM_024452472.2:c.2460T>A, XM_024452472.1:c.2460T>A, XM_017029913.1:c.2460T>A, XM_017029916.1:c.2460T>A, XM_017029917.1:c.2460T>A, XM_017029915.1:c.2460T>A, XM_047442599.1:c.2460T>A, XM_047442600.1:c.2460T>A

Select item 145150232412.

rs1451502324 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:50312889 (GRCh38)
X:50055889 (GRCh37)
Canonical SPDI:: NC_000023.11:50312888:A:G
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.50312889A>G, NW_004070877.1:g.26004A>G, NG_012880.1:g.31716A>G, NC_000023.10:g.50055889A>G, XM_017029914.2:c.3449A>G, XM_017029914.1:c.3449A>G, XM_024452472.2:c.3449A>G, XM_024452472.1:c.3449A>G, XM_017029913.1:c.3449A>G, XM_017029916.1:c.3446A>G, XM_017029915.1:c.3449A>G, XP_016885403.1:p.His1150Arg, XP_024308240.1:p.His1150Arg, XP_016885402.1:p.His1150Arg, XP_016885405.1:p.His1149Arg, XP_016885404.1:p.His1150Arg

Select item 145133996013.

rs1451339960 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:50309687 (GRCh38)
X:50052687 (GRCh37)
Canonical SPDI:: NC_000023.11:50309686:A:G
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00001/1 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.50309687A>G, NW_004070877.1:g.22802A>G, NG_012880.1:g.28514A>G, NM_033031.3:c.1518A>G, NM_033031.2:c.1518A>G, NC_000023.10:g.50052687A>G, XM_017029914.2:c.1518A>G, XM_017029914.1:c.1518A>G, XM_024452472.2:c.1518A>G, XM_024452472.1:c.1518A>G, XM_017029913.1:c.1518A>G, XM_017029916.1:c.1518A>G, XM_017029917.1:c.1518A>G, XM_017029915.1:c.1518A>G, XM_047442599.1:c.1518A>G, XM_047442600.1:c.1518A>G

Select item 145099304514.

rs1450993045 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:50309651 (GRCh38)
X:50052651 (GRCh37)
Canonical SPDI:: NC_000023.11:50309650:G:A
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.50309651G>A, NW_004070877.1:g.22766G>A, NG_012880.1:g.28478G>A, NM_033031.3:c.1482G>A, NM_033031.2:c.1482G>A, NC_000023.10:g.50052651G>A, XM_017029914.2:c.1482G>A, XM_017029914.1:c.1482G>A, XM_024452472.2:c.1482G>A, XM_024452472.1:c.1482G>A, XM_017029913.1:c.1482G>A, XM_017029916.1:c.1482G>A, XM_017029917.1:c.1482G>A, XM_017029915.1:c.1482G>A, XM_047442599.1:c.1482G>A, XM_047442600.1:c.1482G>A

Select item 145037930615.

rs1450379306 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:50308802 (GRCh38)
X:50051802 (GRCh37)
Canonical SPDI:: NC_000023.11:50308801:G:T
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000005/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.50308802G>T, NW_004070877.1:g.21917G>T, NG_012880.1:g.27629G>T, NM_033031.3:c.633G>T, NM_033031.2:c.633G>T, NC_000023.10:g.50051802G>T, XM_017029914.2:c.633G>T, XM_017029914.1:c.633G>T, XM_024452472.2:c.633G>T, XM_024452472.1:c.633G>T, XM_017029913.1:c.633G>T, XM_017029916.1:c.633G>T, XM_017029917.1:c.633G>T, XM_017029915.1:c.633G>T, XM_047442599.1:c.633G>T, XM_047442600.1:c.633G>T, NP_149020.2:p.Met211Ile, XP_016885403.1:p.Met211Ile, XP_024308240.1:p.Met211Ile, XP_016885402.1:p.Met211Ile, XP_016885405.1:p.Met211Ile, XP_016885406.1:p.Met211Ile, XP_016885404.1:p.Met211Ile, XP_047298555.1:p.Met211Ile, XP_047298556.1:p.Met211Ile

Select item 144998116116.

rs1449981161 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:50311184 (GRCh38)
X:50054184 (GRCh37)
Canonical SPDI:: NC_000023.11:50311183:G:A
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000023.11:g.50311184G>A, NW_004070877.1:g.24299G>A, NG_012880.1:g.30011G>A, NM_033031.3:c.3015G>A, NM_033031.2:c.3015G>A, NC_000023.10:g.50054184G>A, XM_017029914.2:c.3015G>A, XM_017029914.1:c.3015G>A, XM_024452472.2:c.3015G>A, XM_024452472.1:c.3015G>A, XM_017029913.1:c.3015G>A, XM_017029916.1:c.3015G>A, XM_017029917.1:c.3015G>A, XM_017029915.1:c.3015G>A, XM_047442599.1:c.3015G>A, XM_047442600.1:c.3015G>A

Select item 144729905117.

rs1447299051 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:50346710 (GRCh38)
X:50089709 (GRCh37)
Canonical SPDI:: NC_000023.11:50346709:G:A
Gene:: CCNB3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.50346710G>A, NW_004070877.1:g.59825G>A, NG_012880.1:g.65536G>A, NM_033670.4:c.401G>A, NM_033670.3:c.401G>A, NM_033670.2:c.401G>A, NM_033031.3:c.3713G>A, NM_033031.2:c.3713G>A, NC_000023.10:g.50089709G>A, XM_017029914.2:c.3740G>A, XM_017029914.1:c.3740G>A, XM_024452472.2:c.3740G>A, XM_024452472.1:c.3740G>A, XM_017029913.1:c.3740G>A, XM_017029916.1:c.3737G>A, XM_017029917.1:c.3716G>A, XM_017029915.1:c.3740G>A, XM_047442599.1:c.3716G>A, XM_047442600.1:c.3713G>A, NM_033671.1:c.*385G>A, NP_391990.1:p.Arg134Gln, NP_149020.2:p.Arg1238Gln, XP_016885403.1:p.Arg1247Gln, XP_024308240.1:p.Arg1247Gln, XP_016885402.1:p.Arg1247Gln, XP_016885405.1:p.Arg1246Gln, XP_016885406.1:p.Arg1239Gln, XP_016885404.1:p.Arg1247Gln, XP_047298555.1:p.Arg1239Gln, XP_047298556.1:p.Arg1238Gln

Select item 144217302618.

rs1442173026 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:50308935 (GRCh38)
X:50051935 (GRCh37)
Canonical SPDI:: NC_000023.11:50308934:A:G
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/2 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
G=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.50308935A>G, NW_004070877.1:g.22050A>G, NG_012880.1:g.27762A>G, NM_033031.3:c.766A>G, NM_033031.2:c.766A>G, NC_000023.10:g.50051935A>G, XM_017029914.2:c.766A>G, XM_017029914.1:c.766A>G, XM_024452472.2:c.766A>G, XM_024452472.1:c.766A>G, XM_017029913.1:c.766A>G, XM_017029916.1:c.766A>G, XM_017029917.1:c.766A>G, XM_017029915.1:c.766A>G, XM_047442599.1:c.766A>G, XM_047442600.1:c.766A>G, NP_149020.2:p.Met256Val, XP_016885403.1:p.Met256Val, XP_024308240.1:p.Met256Val, XP_016885402.1:p.Met256Val, XP_016885405.1:p.Met256Val, XP_016885406.1:p.Met256Val, XP_016885404.1:p.Met256Val, XP_047298555.1:p.Met256Val, XP_047298556.1:p.Met256Val

Select item 144157184919.

rs1441571849 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:50294865 (GRCh38)
X:50037865 (GRCh37)
Canonical SPDI:: NC_000023.11:50294864:T:G
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000685/2 (KOREAN)
HGVS:: NC_000023.11:g.50294865T>G, NW_004070877.1:g.7980T>G, NG_012880.1:g.13692T>G, NM_033031.3:c.207T>G, NM_033031.2:c.207T>G, NC_000023.10:g.50037865T>G, XM_017029914.2:c.207T>G, XM_017029914.1:c.207T>G, XM_024452472.2:c.207T>G, XM_024452472.1:c.207T>G, XM_017029913.1:c.207T>G, XM_017029916.1:c.207T>G, XM_017029917.1:c.207T>G, XM_017029915.1:c.207T>G, XM_047442599.1:c.207T>G, XM_047442600.1:c.207T>G, NM_033671.1:c.207T>G

Select item 143771466420.

rs1437714664 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:50310520 (GRCh38)
X:50053520 (GRCh37)
Canonical SPDI:: NC_000023.11:50310519:C:T
Gene:: CCNB3 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.50310520C>T, NW_004070877.1:g.23635C>T, NG_012880.1:g.29347C>T, NM_033031.3:c.2351C>T, NM_033031.2:c.2351C>T, NC_000023.10:g.50053520C>T, XM_017029914.2:c.2351C>T, XM_017029914.1:c.2351C>T, XM_024452472.2:c.2351C>T, XM_024452472.1:c.2351C>T, XM_017029913.1:c.2351C>T, XM_017029916.1:c.2351C>T, XM_017029917.1:c.2351C>T, XM_017029915.1:c.2351C>T, XM_047442599.1:c.2351C>T, XM_047442600.1:c.2351C>T, NP_149020.2:p.Ala784Val, XP_016885403.1:p.Ala784Val, XP_024308240.1:p.Ala784Val, XP_016885402.1:p.Ala784Val, XP_016885405.1:p.Ala784Val, XP_016885406.1:p.Ala784Val, XP_016885404.1:p.Ala784Val, XP_047298555.1:p.Ala784Val, XP_047298556.1:p.Ala784Val

dbSNP

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