SNP Links for Protein (Select 767985476) - SNP

Links from Protein

Items: 1 to 20 of 218

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Select item 14878171201.

rs1487817120 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:78293218 (GRCh38)
15:78585560 (GRCh37)
Canonical SPDI:: NC_000015.10:78293217:G:C
Gene:: WDR61 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.78293218G>C, NC_000015.9:g.78585560G>C, XM_011522094.3:c.95C>G, XM_011522094.2:c.95C>G, XM_011522094.1:c.95C>G, XM_017022637.3:c.95C>G, XM_017022637.2:c.95C>G, XM_017022637.1:c.95C>G, NM_025234.3:c.95C>G, NM_025234.2:c.95C>G, NM_025234.1:c.95C>G, NM_001303247.2:c.95C>G, NM_001303247.1:c.95C>G, XP_011520396.1:p.Ser32Cys, XP_016878126.1:p.Ser32Cys, NP_079510.1:p.Ser32Cys, NP_001290176.1:p.Ser32Cys

Select item 14863924442.

rs1486392444 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 15:78293233 (GRCh38)
15:78585575 (GRCh37)
Canonical SPDI:: NC_000015.10:78293232:T:A
Gene:: WDR61 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.78293233T>A, NC_000015.9:g.78585575T>A, XM_011522094.3:c.80A>T, XM_011522094.2:c.80A>T, XM_011522094.1:c.80A>T, XM_017022637.3:c.80A>T, XM_017022637.2:c.80A>T, XM_017022637.1:c.80A>T, NM_025234.3:c.80A>T, NM_025234.2:c.80A>T, NM_025234.1:c.80A>T, NM_001303247.2:c.80A>T, NM_001303247.1:c.80A>T, XP_011520396.1:p.Asn27Ile, XP_016878126.1:p.Asn27Ile, NP_079510.1:p.Asn27Ile, NP_001290176.1:p.Asn27Ile

Select item 14862725203.

rs1486272520 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:78289680 (GRCh38)
15:78582022 (GRCh37)
Canonical SPDI:: NC_000015.10:78289679:G:T
Gene:: WDR61 (Varview)
Functional Consequence:: 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.78289680G>T, NC_000015.9:g.78582022G>T, XM_011522094.3:c.501C>A, XM_011522094.2:c.501C>A, XM_011522094.1:c.501C>A, XM_017022637.3:c.501C>A, XM_017022637.2:c.501C>A, XM_017022637.1:c.501C>A, NM_025234.3:c.501C>A, NM_025234.2:c.501C>A, NM_025234.1:c.501C>A, NM_001303247.2:c.501C>A, NM_001303247.1:c.501C>A, NM_001303248.2:c.222C>A, NM_001303248.1:c.222C>A

Select item 14858929534.

rs1485892953 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:78286101 (GRCh38)
15:78578443 (GRCh37)
Canonical SPDI:: NC_000015.10:78286100:C:G
Gene:: WDR61 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.78286101C>G, NC_000015.9:g.78578443C>G, XM_011522094.3:c.689G>C, XM_011522094.2:c.689G>C, XM_011522094.1:c.689G>C, XM_017022637.3:c.689G>C, XM_017022637.2:c.689G>C, XM_017022637.1:c.689G>C, NM_025234.3:c.689G>C, NM_025234.2:c.689G>C, NM_025234.1:c.689G>C, NM_001303247.2:c.689G>C, NM_001303247.1:c.689G>C, NM_001303248.2:c.410G>C, NM_001303248.1:c.410G>C, XP_011520396.1:p.Gly230Ala, XP_016878126.1:p.Gly230Ala, NP_079510.1:p.Gly230Ala, NP_001290176.1:p.Gly230Ala, NP_001290177.1:p.Gly137Ala

Select item 14827910735.

rs1482791073 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:78293222 (GRCh38)
15:78585564 (GRCh37)
Canonical SPDI:: NC_000015.10:78293221:T:C
Gene:: WDR61 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.78293222T>C, NC_000015.9:g.78585564T>C, XM_011522094.3:c.91A>G, XM_011522094.2:c.91A>G, XM_011522094.1:c.91A>G, XM_017022637.3:c.91A>G, XM_017022637.2:c.91A>G, XM_017022637.1:c.91A>G, NM_025234.3:c.91A>G, NM_025234.2:c.91A>G, NM_025234.1:c.91A>G, NM_001303247.2:c.91A>G, NM_001303247.1:c.91A>G, XP_011520396.1:p.Asn31Asp, XP_016878126.1:p.Asn31Asp, NP_079510.1:p.Asn31Asp, NP_001290176.1:p.Asn31Asp

Select item 14791724856.

rs1479172485 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:78293259 (GRCh38)
15:78585601 (GRCh37)
Canonical SPDI:: NC_000015.10:78293258:G:C
Gene:: WDR61 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.78293259G>C, NC_000015.9:g.78585601G>C, XM_011522094.3:c.54C>G, XM_011522094.2:c.54C>G, XM_011522094.1:c.54C>G, XM_017022637.3:c.54C>G, XM_017022637.2:c.54C>G, XM_017022637.1:c.54C>G, NM_025234.3:c.54C>G, NM_025234.2:c.54C>G, NM_025234.1:c.54C>G, NM_001303247.2:c.54C>G, NM_001303247.1:c.54C>G

Select item 14787626737.

rs1478762673 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:78292659 (GRCh38)
15:78585001 (GRCh37)
Canonical SPDI:: NC_000015.10:78292658:G:T
Gene:: WDR61 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.78292659G>T, NC_000015.9:g.78585001G>T, XM_011522094.3:c.276C>A, XM_011522094.2:c.276C>A, XM_011522094.1:c.276C>A, XM_017022637.3:c.276C>A, XM_017022637.2:c.276C>A, XM_017022637.1:c.276C>A, NM_025234.3:c.276C>A, NM_025234.2:c.276C>A, NM_025234.1:c.276C>A, NM_001303247.2:c.276C>A, NM_001303247.1:c.276C>A, XP_011520396.1:p.Asp92Glu, XP_016878126.1:p.Asp92Glu, NP_079510.1:p.Asp92Glu, NP_001290176.1:p.Asp92Glu

Select item 14758894138.

rs1475889413 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:78285325 (GRCh38)
15:78577667 (GRCh37)
Canonical SPDI:: NC_000015.10:78285324:C:T
Gene:: WDR61 (Varview)
Functional Consequence:: 3_prime_UTR_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.78285325C>T, NC_000015.9:g.78577667C>T, XM_011522094.3:c.764G>A, XM_011522094.2:c.764G>A, XM_011522094.1:c.764G>A, XM_017022637.3:c.*336G>A, XM_017022637.2:c.*336G>A, XM_017022637.1:c.*336G>A, NM_025234.3:c.764G>A, NM_025234.2:c.764G>A, NM_025234.1:c.764G>A, NM_001303247.2:c.764G>A, NM_001303247.1:c.764G>A, NM_001303248.2:c.485G>A, NM_001303248.1:c.485G>A, XP_011520396.1:p.Ser255Asn, NP_079510.1:p.Ser255Asn, NP_001290176.1:p.Ser255Asn, NP_001290177.1:p.Ser162Asn

Select item 14714148769.

rs1471414876 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:78290026 (GRCh38)
15:78582368 (GRCh37)
Canonical SPDI:: NC_000015.10:78290025:G:A
Gene:: WDR61 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000015.10:g.78290026G>A, NC_000015.9:g.78582368G>A, XM_011522094.3:c.393C>T, XM_011522094.2:c.393C>T, XM_011522094.1:c.393C>T, XM_017022637.3:c.393C>T, XM_017022637.2:c.393C>T, XM_017022637.1:c.393C>T, NM_025234.3:c.393C>T, NM_025234.2:c.393C>T, NM_025234.1:c.393C>T, NM_001303247.2:c.393C>T, NM_001303247.1:c.393C>T, NM_001303248.2:c.114C>T, NM_001303248.1:c.114C>T

Select item 146789968710.

rs1467899687 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:78288348 (GRCh38)
15:78580690 (GRCh37)
Canonical SPDI:: NC_000015.10:78288347:G:A
Gene:: WDR61 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.78288348G>A, NC_000015.9:g.78580690G>A, XM_011522094.3:c.597C>T, XM_011522094.2:c.597C>T, XM_011522094.1:c.597C>T, XM_017022637.3:c.597C>T, XM_017022637.2:c.597C>T, XM_017022637.1:c.597C>T, NM_025234.3:c.597C>T, NM_025234.2:c.597C>T, NM_025234.1:c.597C>T, NM_001303247.2:c.597C>T, NM_001303247.1:c.597C>T, NM_001303248.2:c.318C>T, NM_001303248.1:c.318C>T

Select item 146440028211.

rs1464400282 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:78292670 (GRCh38)
15:78585012 (GRCh37)
Canonical SPDI:: NC_000015.10:78292669:G:A
Gene:: WDR61 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000056/2 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
HGVS:: NC_000015.10:g.78292670G>A, NC_000015.9:g.78585012G>A, XM_011522094.3:c.265C>T, XM_011522094.2:c.265C>T, XM_011522094.1:c.265C>T, XM_017022637.3:c.265C>T, XM_017022637.2:c.265C>T, XM_017022637.1:c.265C>T, NM_025234.3:c.265C>T, NM_025234.2:c.265C>T, NM_025234.1:c.265C>T, NM_001303247.2:c.265C>T, NM_001303247.1:c.265C>T, XP_011520396.1:p.Arg89Cys, XP_016878126.1:p.Arg89Cys, NP_079510.1:p.Arg89Cys, NP_001290176.1:p.Arg89Cys

Select item 145443356012.

rs1454433560 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:78292705 (GRCh38)
15:78585047 (GRCh37)
Canonical SPDI:: NC_000015.10:78292704:G:C
Gene:: WDR61 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.78292705G>C, NC_000015.9:g.78585047G>C, XM_011522094.3:c.230C>G, XM_011522094.2:c.230C>G, XM_011522094.1:c.230C>G, XM_017022637.3:c.230C>G, XM_017022637.2:c.230C>G, XM_017022637.1:c.230C>G, NM_025234.3:c.230C>G, NM_025234.2:c.230C>G, NM_025234.1:c.230C>G, NM_001303247.2:c.230C>G, NM_001303247.1:c.230C>G, XP_011520396.1:p.Pro77Arg, XP_016878126.1:p.Pro77Arg, NP_079510.1:p.Pro77Arg, NP_001290176.1:p.Pro77Arg

Select item 144719285913.

rs1447192859 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:78283443 (GRCh38)
15:78575785 (GRCh37)
Canonical SPDI:: NC_000015.10:78283442:A:C
Gene:: WDR61 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000028/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.78283443A>C, NC_000015.9:g.78575785A>C, XM_011522094.3:c.907T>G, XM_011522094.2:c.907T>G, XM_011522094.1:c.907T>G, NM_025234.3:c.907T>G, NM_025234.2:c.907T>G, NM_025234.1:c.907T>G, NM_001303247.2:c.907T>G, NM_001303247.1:c.907T>G, NM_001303248.2:c.628T>G, NM_001303248.1:c.628T>G, XP_011520396.1:p.Cys303Gly, NP_079510.1:p.Cys303Gly, NP_001290176.1:p.Cys303Gly, NP_001290177.1:p.Cys210Gly

Select item 144090775814.

rs1440907758 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 15:78288323 (GRCh38)
15:78580665 (GRCh37)
Canonical SPDI:: NC_000015.10:78288322:C:
Gene:: WDR61 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
HGVS:: NC_000015.10:g.78288323del, NC_000015.9:g.78580665del, XM_011522094.3:c.622del, XM_011522094.2:c.622del, XM_011522094.1:c.622del, XM_017022637.3:c.622del, XM_017022637.2:c.622del, XM_017022637.1:c.622del, NM_025234.3:c.622del, NM_025234.2:c.622del, NM_025234.1:c.622del, NM_001303247.2:c.622del, NM_001303247.1:c.622del, NM_001303248.2:c.343del, NM_001303248.1:c.343del, XP_011520396.1:p.Ala208fs, XP_016878126.1:p.Ala208fs, NP_079510.1:p.Ala208fs, NP_001290176.1:p.Ala208fs, NP_001290177.1:p.Ala115fs

Select item 143935414615.

rs1439354146 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:78288293 (GRCh38)
15:78580635 (GRCh37)
Canonical SPDI:: NC_000015.10:78288292:C:A
Gene:: WDR61 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000015.10:g.78288293C>A, NC_000015.9:g.78580635C>A, XM_011522094.3:c.652G>T, XM_011522094.2:c.652G>T, XM_011522094.1:c.652G>T, XM_017022637.3:c.652G>T, XM_017022637.2:c.652G>T, XM_017022637.1:c.652G>T, NM_025234.3:c.652G>T, NM_025234.2:c.652G>T, NM_025234.1:c.652G>T, NM_001303247.2:c.652G>T, NM_001303247.1:c.652G>T, NM_001303248.2:c.373G>T, NM_001303248.1:c.373G>T, XP_011520396.1:p.Asp218Tyr, XP_016878126.1:p.Asp218Tyr, NP_079510.1:p.Asp218Tyr, NP_001290176.1:p.Asp218Tyr, NP_001290177.1:p.Asp125Tyr

Select item 143274433816.

rs1432744338 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:78289689 (GRCh38)
15:78582031 (GRCh37)
Canonical SPDI:: NC_000015.10:78289688:G:A
Gene:: WDR61 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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.78289689G>A, NC_000015.9:g.78582031G>A, XM_011522094.3:c.492C>T, XM_011522094.2:c.492C>T, XM_011522094.1:c.492C>T, XM_017022637.3:c.492C>T, XM_017022637.2:c.492C>T, XM_017022637.1:c.492C>T, NM_025234.3:c.492C>T, NM_025234.2:c.492C>T, NM_025234.1:c.492C>T, NM_001303247.2:c.492C>T, NM_001303247.1:c.492C>T, NM_001303248.2:c.213C>T, NM_001303248.1:c.213C>T

Select item 143123493017.

rs1431234930 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:78293244 (GRCh38)
15:78585586 (GRCh37)
Canonical SPDI:: NC_000015.10:78293243:A:G
Gene:: WDR61 (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.78293244A>G, NC_000015.9:g.78585586A>G, XM_011522094.3:c.69T>C, XM_011522094.2:c.69T>C, XM_011522094.1:c.69T>C, XM_017022637.3:c.69T>C, XM_017022637.2:c.69T>C, XM_017022637.1:c.69T>C, NM_025234.3:c.69T>C, NM_025234.2:c.69T>C, NM_025234.1:c.69T>C, NM_001303247.2:c.69T>C, NM_001303247.1:c.69T>C

Select item 142929654518.

rs1429296545 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:78292664 (GRCh38)
15:78585006 (GRCh37)
Canonical SPDI:: NC_000015.10:78292663:A:C
Gene:: WDR61 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000015.10:g.78292664A>C, NC_000015.9:g.78585006A>C, XM_011522094.3:c.271T>G, XM_011522094.2:c.271T>G, XM_011522094.1:c.271T>G, XM_017022637.3:c.271T>G, XM_017022637.2:c.271T>G, XM_017022637.1:c.271T>G, NM_025234.3:c.271T>G, NM_025234.2:c.271T>G, NM_025234.1:c.271T>G, NM_001303247.2:c.271T>G, NM_001303247.1:c.271T>G, XP_011520396.1:p.Trp91Gly, XP_016878126.1:p.Trp91Gly, NP_079510.1:p.Trp91Gly, NP_001290176.1:p.Trp91Gly

Select item 142259064419.

rs1422590644 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTT>- [Show Flanks]
Chromosome:: 15:78293229 (GRCh38)
15:78585571 (GRCh37)
Canonical SPDI:: NC_000015.10:78293225:CTTCTT:CTT
Gene:: WDR61 (Varview)
Functional Consequence:: inframe_deletion,intron_variant,coding_sequence_variant
HGVS:: NC_000015.10:g.78293226CTT[1], NC_000015.9:g.78585568CTT[1], XM_011522094.3:c.82AAG[1], XM_011522094.2:c.82AAG[1], XM_011522094.1:c.82AAG[1], XM_017022637.3:c.82AAG[1], XM_017022637.2:c.82AAG[1], XM_017022637.1:c.82AAG[1], NM_025234.3:c.82AAG[1], NM_025234.2:c.82AAG[1], NM_025234.1:c.82AAG[1], NM_001303247.2:c.82AAG[1], NM_001303247.1:c.82AAG[1], XP_011520396.1:p.Lys29del, XP_016878126.1:p.Lys29del, NP_079510.1:p.Lys29del, NP_001290176.1:p.Lys29del

Select item 141747048420.

rs1417470484 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:78293175 (GRCh38)
15:78585517 (GRCh37)
Canonical SPDI:: NC_000015.10:78293174:G:C
Gene:: WDR61 (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_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.78293175G>C, NC_000015.9:g.78585517G>C, XM_011522094.3:c.138C>G, XM_011522094.2:c.138C>G, XM_011522094.1:c.138C>G, XM_017022637.3:c.138C>G, XM_017022637.2:c.138C>G, XM_017022637.1:c.138C>G, NM_025234.3:c.138C>G, NM_025234.2:c.138C>G, NM_025234.1:c.138C>G, NM_001303247.2:c.138C>G, NM_001303247.1:c.138C>G

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