SNP Links for Protein (Select 4507321) - SNP

Links from Protein

Items: 1 to 20 of 143

<< First< Prev

Page of 8

Next >Last >>

Select item 14826719201.

rs1482671920 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48700219 (GRCh38)
X:48558610 (GRCh37)
Canonical SPDI:: NC_000023.11:48700218:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.48700219C>T, NW_004070880.2:g.939648C>T, NG_012530.2:g.8480C>T, NM_003173.4:c.294C>T, NM_003173.3:c.294C>T, NM_003173.2:c.294C>T, NM_001282166.2:c.327C>T, NM_001282166.1:c.327C>T, NC_000023.10:g.48558610C>T

Select item 14723389782.

rs1472338978 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48700424 (GRCh38)
X:48558815 (GRCh37)
Canonical SPDI:: NC_000023.11:48700423:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000043/1 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000016/3 (GnomAD_exomes)
HGVS:: NC_000023.11:g.48700424C>T, NW_004070880.2:g.939853C>T, NG_012530.2:g.8685C>T, NM_003173.4:c.499C>T, NM_003173.3:c.499C>T, NM_003173.2:c.499C>T, NM_001282166.2:c.532C>T, NM_001282166.1:c.532C>T, NC_000023.10:g.48558815C>T, NP_003164.1:p.Arg167Cys, NP_001269095.1:p.Arg178Cys

Select item 14659495023.

rs1465949502 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:48700496 (GRCh38)
X:48558887 (GRCh37)
Canonical SPDI:: NC_000023.11:48700495:A:G
Gene:: SUV39H1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.48700496A>G, NW_004070880.2:g.939925A>G, NG_012530.2:g.8757A>G, NM_003173.4:c.571A>G, NM_003173.3:c.571A>G, NM_003173.2:c.571A>G, NM_001282166.2:c.604A>G, NM_001282166.1:c.604A>G, NC_000023.10:g.48558887A>G, NP_003164.1:p.Thr191Ala, NP_001269095.1:p.Thr202Ala

Select item 14639848014.

rs1463984801 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48706588 (GRCh38)
X:48564979 (GRCh37)
Canonical SPDI:: NC_000023.11:48706587:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.48706588C>T, NW_004070880.2:g.946017C>T, NG_012530.2:g.14849C>T, NM_003173.4:c.1066C>T, NM_003173.3:c.1066C>T, NM_003173.2:c.1066C>T, NM_001282166.2:c.1099C>T, NM_001282166.1:c.1099C>T, NC_000023.10:g.48564979C>T, NP_003164.1:p.Arg356Trp, NP_001269095.1:p.Arg367Trp

Select item 14579988375.

rs1457998837 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:48700397 (GRCh38)
X:48558788 (GRCh37)
Canonical SPDI:: NC_000023.11:48700396:C:A,NC_000023.11:48700396:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000005/1 (GnomAD_exomes)
T=0.000019/5 (TOPMED)
T=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.48700397C>A, NC_000023.11:g.48700397C>T, NW_004070880.2:g.939826C>A, NW_004070880.2:g.939826C>T, NG_012530.2:g.8658C>A, NG_012530.2:g.8658C>T, NM_003173.4:c.472C>A, NM_003173.4:c.472C>T, NM_003173.3:c.472C>A, NM_003173.3:c.472C>T, NM_003173.2:c.472C>A, NM_003173.2:c.472C>T, NM_001282166.2:c.505C>A, NM_001282166.2:c.505C>T, NM_001282166.1:c.505C>A, NM_001282166.1:c.505C>T, NC_000023.10:g.48558788C>A, NC_000023.10:g.48558788C>T, NP_003164.1:p.Arg158Trp, NP_001269095.1:p.Arg169Trp

Select item 14348783416.

rs1434878341 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48699024 (GRCh38)
X:48557415 (GRCh37)
Canonical SPDI:: NC_000023.11:48699023:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.48699024C>T, NW_004070880.2:g.938453C>T, NG_012530.2:g.7285C>T, NM_003173.4:c.142C>T, NM_003173.3:c.142C>T, NM_003173.2:c.142C>T, NM_001282166.2:c.175C>T, NM_001282166.1:c.175C>T, NC_000023.10:g.48557415C>T

Select item 14233094577.

rs1423309457 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48700154 (GRCh38)
X:48558545 (GRCh37)
Canonical SPDI:: NC_000023.11:48700153:C:T
Gene:: SUV39H1 (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_000023.11:g.48700154C>T, NW_004070880.2:g.939583C>T, NG_012530.2:g.8415C>T, NM_003173.4:c.229C>T, NM_003173.3:c.229C>T, NM_003173.2:c.229C>T, NM_001282166.2:c.262C>T, NM_001282166.1:c.262C>T, NC_000023.10:g.48558545C>T, NP_003164.1:p.Arg77Trp, NP_001269095.1:p.Arg88Trp

Select item 14165619578.

rs1416561957 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:48700143 (GRCh38)
X:48558534 (GRCh37)
Canonical SPDI:: NC_000023.11:48700142:C:G
Gene:: SUV39H1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.48700143C>G, NW_004070880.2:g.939572C>G, NG_012530.2:g.8404C>G, NM_003173.4:c.218C>G, NM_003173.3:c.218C>G, NM_003173.2:c.218C>G, NM_001282166.2:c.251C>G, NM_001282166.1:c.251C>G, NC_000023.10:g.48558534C>G, NP_003164.1:p.Thr73Ser, NP_001269095.1:p.Thr84Ser

Select item 14010811519.

rs1401081151 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48706560 (GRCh38)
X:48564951 (GRCh37)
Canonical SPDI:: NC_000023.11:48706559:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.48706560C>T, NW_004070880.2:g.945989C>T, NG_012530.2:g.14821C>T, NM_003173.4:c.1038C>T, NM_003173.3:c.1038C>T, NM_003173.2:c.1038C>T, NM_001282166.2:c.1071C>T, NM_001282166.1:c.1071C>T, NC_000023.10:g.48564951C>T

Select item 139546505610.

rs1395465056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48699045 (GRCh38)
X:48557436 (GRCh37)
Canonical SPDI:: NC_000023.11:48699044:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.48699045C>T, NW_004070880.2:g.938474C>T, NG_012530.2:g.7306C>T, NM_003173.4:c.163C>T, NM_003173.3:c.163C>T, NM_003173.2:c.163C>T, NM_001282166.2:c.196C>T, NM_001282166.1:c.196C>T, NC_000023.10:g.48557436C>T, NP_003164.1:p.Arg55Cys, NP_001269095.1:p.Arg66Cys

Select item 139116505611.

rs1391165056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48700401 (GRCh38)
X:48558792 (GRCh37)
Canonical SPDI:: NC_000023.11:48700400:C:T
Gene:: SUV39H1 (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_000023.11:g.48700401C>T, NW_004070880.2:g.939830C>T, NG_012530.2:g.8662C>T, NM_003173.4:c.476C>T, NM_003173.3:c.476C>T, NM_003173.2:c.476C>T, NM_001282166.2:c.509C>T, NM_001282166.1:c.509C>T, NC_000023.10:g.48558792C>T, NP_003164.1:p.Ala159Val, NP_001269095.1:p.Ala170Val

Select item 137029713612.

rs1370297136 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGA [Show Flanks]
Chromosome:: X:48700094 (GRCh38)
X:48558486 (GRCh37)
Canonical SPDI:: NC_000023.11:48700094:AGGA:AGGAGGA
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_insertion
Validated:: by frequency,by alfa,by cluster
MAF:: AGGAGGA=0./0 (ALFA)
AGG=0.00001/1 (GnomAD)
AGG=0.000011/3 (TOPMED)
AGG=0.000098/1 (GoESP)
HGVS:: NC_000023.11:g.48700096_48700098dup, NW_004070880.2:g.939525_939527dup, NG_012530.2:g.8357_8359dup, NM_003173.4:c.171_173dup, NM_003173.3:c.171_173dup, NM_003173.2:c.171_173dup, NM_001282166.2:c.204_206dup, NM_001282166.1:c.204_206dup, NC_000023.10:g.48558487_48558489dup, NP_003164.1:p.Glu58dup, NP_001269095.1:p.Glu69dup

Select item 136446557713.

rs1364465577 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: X:48698981 (GRCh38)
X:48557372 (GRCh37)
Canonical SPDI:: NC_000023.11:48698980:C:G,NC_000023.11:48698980:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
G=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.48698981C>G, NC_000023.11:g.48698981C>T, NW_004070880.2:g.938410C>G, NW_004070880.2:g.938410C>T, NG_012530.2:g.7242C>G, NG_012530.2:g.7242C>T, NM_003173.4:c.99C>G, NM_003173.4:c.99C>T, NM_003173.3:c.99C>G, NM_003173.3:c.99C>T, NM_003173.2:c.99C>G, NM_003173.2:c.99C>T, NM_001282166.2:c.132C>G, NM_001282166.2:c.132C>T, NM_001282166.1:c.132C>G, NM_001282166.1:c.132C>T, NC_000023.10:g.48557372C>G, NC_000023.10:g.48557372C>T

Select item 134662117814.

rs1346621178 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:48707531 (GRCh38)
X:48565922 (GRCh37)
Canonical SPDI:: NC_000023.11:48707530:C:T
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.48707531C>T, NW_004070880.2:g.946960C>T, NG_012530.2:g.15792C>T, NM_003173.4:c.1200C>T, NM_003173.3:c.1200C>T, NM_003173.2:c.1200C>T, NM_001282166.2:c.1233C>T, NM_001282166.1:c.1233C>T, NC_000023.10:g.48565922C>T

Select item 133369981415.

rs1333699814 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: X:48700390 (GRCh38)
X:48558781 (GRCh37)
Canonical SPDI:: NC_000023.11:48700389:C:G
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.48700390C>G, NW_004070880.2:g.939819C>G, NG_012530.2:g.8651C>G, NM_003173.4:c.465C>G, NM_003173.3:c.465C>G, NM_003173.2:c.465C>G, NM_001282166.2:c.498C>G, NM_001282166.1:c.498C>G, NC_000023.10:g.48558781C>G

Select item 133349839516.

rs1333498395 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:48706582 (GRCh38)
X:48564973 (GRCh37)
Canonical SPDI:: NC_000023.11:48706581:A:G
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000096/2 (ALFA)
G=0.000023/4 (GnomAD_exomes)
G=0.000029/3 (GnomAD)
G=0.000053/14 (TOPMED)
HGVS:: NC_000023.11:g.48706582A>G, NW_004070880.2:g.946011A>G, NG_012530.2:g.14843A>G, NM_003173.4:c.1060A>G, NM_003173.3:c.1060A>G, NM_003173.2:c.1060A>G, NM_001282166.2:c.1093A>G, NM_001282166.1:c.1093A>G, NC_000023.10:g.48564973A>G, NP_003164.1:p.Thr354Ala, NP_001269095.1:p.Thr365Ala

Select item 128394679817.

rs1283946798 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:48700681 (GRCh38)
X:48559072 (GRCh37)
Canonical SPDI:: NC_000023.11:48700680:T:C
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.48700681T>C, NW_004070880.2:g.940110T>C, NG_012530.2:g.8942T>C, NM_003173.4:c.756T>C, NM_003173.3:c.756T>C, NM_003173.2:c.756T>C, NM_001282166.2:c.789T>C, NM_001282166.1:c.789T>C, NC_000023.10:g.48559072T>C

Select item 123055514218.

rs1230555142 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:48700671 (GRCh38)
X:48559062 (GRCh37)
Canonical SPDI:: NC_000023.11:48700670:G:A
Gene:: SUV39H1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000023.11:g.48700671G>A, NW_004070880.2:g.940100G>A, NG_012530.2:g.8932G>A, NM_003173.4:c.746G>A, NM_003173.3:c.746G>A, NM_003173.2:c.746G>A, NM_001282166.2:c.779G>A, NM_001282166.1:c.779G>A, NC_000023.10:g.48559062G>A, NP_003164.1:p.Arg249His, NP_001269095.1:p.Arg260His

Select item 121195800719.

rs1211958007 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:48700233 (GRCh38)
X:48558624 (GRCh37)
Canonical SPDI:: NC_000023.11:48700232:G:A
Gene:: SUV39H1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.00001/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000023.11:g.48700233G>A, NW_004070880.2:g.939662G>A, NG_012530.2:g.8494G>A, NM_003173.4:c.308G>A, NM_003173.3:c.308G>A, NM_003173.2:c.308G>A, NM_001282166.2:c.341G>A, NM_001282166.1:c.341G>A, NC_000023.10:g.48558624G>A, NP_003164.1:p.Arg103Gln, NP_001269095.1:p.Arg114Gln

Select item 117988015120.

rs1179880151 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:48700184 (GRCh38)
X:48558575 (GRCh37)
Canonical SPDI:: NC_000023.11:48700183:A:G
Gene:: SUV39H1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.48700184A>G, NW_004070880.2:g.939613A>G, NG_012530.2:g.8445A>G, NM_003173.4:c.259A>G, NM_003173.3:c.259A>G, NM_003173.2:c.259A>G, NM_001282166.2:c.292A>G, NM_001282166.1:c.292A>G, NC_000023.10:g.48558575A>G, NP_003164.1:p.Lys87Glu, NP_001269095.1:p.Lys98Glu

<< First< Prev

Page of 8

Next >Last >>

dbSNP

Result Filters

Clinical Significance

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 143

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity