SNP Links for Protein (Select 4506387) - SNP

Links from Protein

Items: 1 to 20 of 325

<< First< Prev

Page of 17

Next >Last >>

Select item 14908271201.

rs1490827120 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:107318755 (GRCh38)
9:110081036 (GRCh37)
Canonical SPDI:: NC_000009.12:107318754:C:T
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000009.12:g.107318755C>T, NC_000009.11:g.110081036C>T, NM_002874.5:c.557C>T, NM_002874.4:c.557C>T, NM_001244724.2:c.341C>T, NM_001244724.1:c.341C>T, NM_001244713.1:c.494C>T, NP_002865.1:p.Thr186Met, NP_001231653.1:p.Thr114Met, NP_001231642.1:p.Thr165Met

Select item 14843214412.

rs1484321441 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:107322056 (GRCh38)
9:110084337 (GRCh37)
Canonical SPDI:: NC_000009.12:107322055:C:G
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.107322056C>G, NC_000009.11:g.110084337C>G, NM_002874.5:c.755C>G, NM_002874.4:c.755C>G, NM_001244724.2:c.539C>G, NM_001244724.1:c.539C>G, NM_001244713.1:c.692C>G, NP_002865.1:p.Ser252Cys, NP_001231653.1:p.Ser180Cys, NP_001231642.1:p.Ser231Cys

Select item 14833715943.

rs1483371594 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:107324940 (GRCh38)
9:110087221 (GRCh37)
Canonical SPDI:: NC_000009.12:107324939:A:G
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.107324940A>G, NC_000009.11:g.110087221A>G, NM_002874.5:c.1052A>G, NM_002874.4:c.1052A>G, NM_001244724.2:c.836A>G, NM_001244724.1:c.836A>G, NM_001244713.1:c.989A>G, NP_002865.1:p.Glu351Gly, NP_001231653.1:p.Glu279Gly, NP_001231642.1:p.Glu330Gly

Select item 14817595894.

rs1481759589 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 9:107306574 (GRCh38)
9:110068855 (GRCh37)
Canonical SPDI:: NC_000009.12:107306573:G:T
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.107306574G>T, NC_000009.11:g.110068855G>T, NM_002874.5:c.424G>T, NM_002874.4:c.424G>T, NM_001244724.2:c.208G>T, NM_001244724.1:c.208G>T, NM_001244713.1:c.361G>T, NP_002865.1:p.Ala142Ser, NP_001231653.1:p.Ala70Ser, NP_001231642.1:p.Ala121Ser

Select item 14817330805.

rs1481733080 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:107283682 (GRCh38)
9:110045963 (GRCh37)
Canonical SPDI:: NC_000009.12:107283681:A:G
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,missense_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000028/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.107283682A>G, NC_000009.11:g.110045963A>G, NM_002874.5:c.53A>G, NM_002874.4:c.53A>G, NP_002865.1:p.Asp18Gly

Select item 14789933006.

rs1478993300 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:107311684 (GRCh38)
9:110073965 (GRCh37)
Canonical SPDI:: NC_000009.12:107311683:C:T
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.107311684C>T, NC_000009.11:g.110073965C>T, NM_002874.5:c.500C>T, NM_002874.4:c.500C>T, NM_001244724.2:c.284C>T, NM_001244724.1:c.284C>T, NM_001244713.1:c.437C>T, NP_002865.1:p.Thr167Ile, NP_001231653.1:p.Thr95Ile, NP_001231642.1:p.Thr146Ile

Select item 14773600387.

rs1477360038 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:107324866 (GRCh38)
9:110087147 (GRCh37)
Canonical SPDI:: NC_000009.12:107324865:G:C
Gene:: RAD23B (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_000009.12:g.107324866G>C, NC_000009.11:g.110087147G>C, NM_002874.5:c.978G>C, NM_002874.4:c.978G>C, NM_001244724.2:c.762G>C, NM_001244724.1:c.762G>C, NM_001244713.1:c.915G>C, NP_002865.1:p.Gln326His, NP_001231653.1:p.Gln254His, NP_001231642.1:p.Gln305His

Select item 14729076688.

rs1472907668 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:107311709 (GRCh38)
9:110073990 (GRCh37)
Canonical SPDI:: NC_000009.12:107311708:C:T
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000009/2 (GnomAD_exomes)
T=0.000021/3 (GnomAD)
T=0.000049/13 (TOPMED)
HGVS:: NC_000009.12:g.107311709C>T, NC_000009.11:g.110073990C>T, NM_002874.5:c.525C>T, NM_002874.4:c.525C>T, NM_001244724.2:c.309C>T, NM_001244724.1:c.309C>T, NM_001244713.1:c.462C>T

Select item 14715048329.

rs1471504832 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:107318863 (GRCh38)
9:110081144 (GRCh37)
Canonical SPDI:: NC_000009.12:107318862:T:C
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.107318863T>C, NC_000009.11:g.110081144T>C, NM_002874.5:c.665T>C, NM_002874.4:c.665T>C, NM_001244724.2:c.449T>C, NM_001244724.1:c.449T>C, NM_001244713.1:c.602T>C, NP_002865.1:p.Val222Ala, NP_001231653.1:p.Val150Ala, NP_001231642.1:p.Val201Ala

Select item 146998748410.

rs1469987484 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:107306527 (GRCh38)
9:110068808 (GRCh37)
Canonical SPDI:: NC_000009.12:107306526:T:A
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.107306527T>A, NC_000009.11:g.110068808T>A, NM_002874.5:c.377T>A, NM_002874.4:c.377T>A, NM_001244724.2:c.161T>A, NM_001244724.1:c.161T>A, NM_001244713.1:c.314T>A, NP_002865.1:p.Ile126Asn, NP_001231653.1:p.Ile54Asn, NP_001231642.1:p.Ile105Asn

Select item 146847478011.

rs1468474780 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:107325001 (GRCh38)
9:110087282 (GRCh37)
Canonical SPDI:: NC_000009.12:107325000:A:C
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.107325001A>C, NC_000009.11:g.110087282A>C, NM_002874.5:c.1113A>C, NM_002874.4:c.1113A>C, NM_001244724.2:c.897A>C, NM_001244724.1:c.897A>C, NM_001244713.1:c.1050A>C, NP_002865.1:p.Glu371Asp, NP_001231653.1:p.Glu299Asp, NP_001231642.1:p.Glu350Asp

Select item 146539057612.

rs1465390576 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:107283651 (GRCh38)
9:110045932 (GRCh37)
Canonical SPDI:: NC_000009.12:107283650:C:G
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,upstream_transcript_variant,missense_variant
HGVS:: NC_000009.12:g.107283651C>G, NC_000009.11:g.110045932C>G, NM_002874.5:c.22C>G, NM_002874.4:c.22C>G, NP_002865.1:p.Leu8Val

Select item 146192034313.

rs1461920343 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:107306500 (GRCh38)
9:110068781 (GRCh37)
Canonical SPDI:: NC_000009.12:107306499:T:C
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.107306500T>C, NC_000009.11:g.110068781T>C, NM_002874.5:c.350T>C, NM_002874.4:c.350T>C, NM_001244724.2:c.134T>C, NM_001244724.1:c.134T>C, NM_001244713.1:c.287T>C, NP_002865.1:p.Leu117Ser, NP_001231653.1:p.Leu45Ser, NP_001231642.1:p.Leu96Ser

Select item 145930295014.

rs1459302950 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 9:107306608 (GRCh38)
9:110068889 (GRCh37)
Canonical SPDI:: NC_000009.12:107306607:C:A,NC_000009.12:107306607:C:G
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000009.12:g.107306608C>A, NC_000009.12:g.107306608C>G, NC_000009.11:g.110068889C>A, NC_000009.11:g.110068889C>G, NM_002874.5:c.458C>A, NM_002874.5:c.458C>G, NM_002874.4:c.458C>A, NM_002874.4:c.458C>G, NM_001244724.2:c.242C>A, NM_001244724.2:c.242C>G, NM_001244724.1:c.242C>A, NM_001244724.1:c.242C>G, NM_001244713.1:c.395C>A, NM_001244713.1:c.395C>G, NP_002865.1:p.Ala153Glu, NP_002865.1:p.Ala153Gly, NP_001231653.1:p.Ala81Glu, NP_001231653.1:p.Ala81Gly, NP_001231642.1:p.Ala132Glu, NP_001231642.1:p.Ala132Gly

Select item 145691153115.

rs1456911531 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:107302111 (GRCh38)
9:110064392 (GRCh37)
Canonical SPDI:: NC_000009.12:107302110:C:T
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000094/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.107302111C>T, NC_000009.11:g.110064392C>T, NM_002874.5:c.225C>T, NM_002874.4:c.225C>T, NM_001244724.2:c.9C>T, NM_001244724.1:c.9C>T, NM_001244713.1:c.162C>T

Select item 145340216316.

rs1453402163 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:107318813 (GRCh38)
9:110081094 (GRCh37)
Canonical SPDI:: NC_000009.12:107318812:G:A
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000009.12:g.107318813G>A, NC_000009.11:g.110081094G>A, NM_002874.5:c.615G>A, NM_002874.4:c.615G>A, NM_001244724.2:c.399G>A, NM_001244724.1:c.399G>A, NM_001244713.1:c.552G>A

Select item 144342526917.

rs1443425269 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:107311692 (GRCh38)
9:110073973 (GRCh37)
Canonical SPDI:: NC_000009.12:107311691:G:A
Gene:: RAD23B (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000009.12:g.107311692G>A, NC_000009.11:g.110073973G>A, NM_002874.5:c.508G>A, NM_002874.4:c.508G>A, NM_001244724.2:c.292G>A, NM_001244724.1:c.292G>A, NM_001244713.1:c.445G>A, NP_002865.1:p.Asp170Asn, NP_001231653.1:p.Asp98Asn, NP_001231642.1:p.Asp149Asn

Select item 144157957418.

rs1441579574 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:107306424 (GRCh38)
9:110068705 (GRCh37)
Canonical SPDI:: NC_000009.12:107306423:G:C
Gene:: RAD23B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.107306424G>C, NC_000009.11:g.110068705G>C, NM_002874.5:c.274G>C, NM_002874.4:c.274G>C, NM_001244724.2:c.58G>C, NM_001244724.1:c.58G>C, NM_001244713.1:c.211G>C, NP_002865.1:p.Ala92Pro, NP_001231653.1:p.Ala20Pro, NP_001231642.1:p.Ala71Pro

Select item 143855820519.

rs1438558205 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 9:107322107 (GRCh38)
9:110084388 (GRCh37)
Canonical SPDI:: NC_000009.12:107322106:C:
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.107322107del, NC_000009.11:g.110084388del, NM_002874.5:c.806del, NM_002874.4:c.806del, NM_001244724.2:c.590del, NM_001244724.1:c.590del, NM_001244713.1:c.743del, NP_002865.1:p.Thr269fs, NP_001231653.1:p.Thr197fs, NP_001231642.1:p.Thr248fs

Select item 143664341020.

rs1436643410 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:107302042 (GRCh38)
9:110064323 (GRCh37)
Canonical SPDI:: NC_000009.12:107302041:C:T
Gene:: RAD23B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.107302042C>T, NC_000009.11:g.110064323C>T, NM_002874.5:c.156C>T, NM_002874.4:c.156C>T, NM_001244724.2:c.-61C>T, NM_001244724.1:c.-61C>T, NM_001244713.1:c.93C>T

<< First< Prev

Page of 17

Next >Last >>

dbSNP

Result Filters

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 325

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity