SNP Links for Protein (Select 22748809) - SNP

Links from Protein

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Select item 14902046731.

rs1490204673 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:20191268 (GRCh38)
1:20517761 (GRCh37)
Canonical SPDI:: NC_000001.11:20191267:A:G
Gene:: UBXN10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.20191268A>G, NC_000001.10:g.20517761A>G, XM_005245742.5:c.707A>G, XM_005245742.4:c.707A>G, XM_005245742.3:c.707A>G, XM_005245742.2:c.707A>G, XM_005245742.1:c.707A>G, NM_152376.5:c.707A>G, NM_152376.4:c.707A>G, NM_152376.3:c.707A>G, XM_011540699.4:c.707A>G, XM_011540699.3:c.707A>G, XM_011540699.2:c.707A>G, XM_011540699.1:c.707A>G, XP_005245799.1:p.Tyr236Cys, NP_689589.1:p.Tyr236Cys, XP_011539001.1:p.Tyr236Cys

Select item 14875162982.

rs1487516298 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:20191226 (GRCh38)
1:20517719 (GRCh37)
Canonical SPDI:: NC_000001.11:20191225:A:G
Gene:: UBXN10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.20191226A>G, NC_000001.10:g.20517719A>G, XM_005245742.5:c.665A>G, XM_005245742.4:c.665A>G, XM_005245742.3:c.665A>G, XM_005245742.2:c.665A>G, XM_005245742.1:c.665A>G, NM_152376.5:c.665A>G, NM_152376.4:c.665A>G, NM_152376.3:c.665A>G, XM_011540699.4:c.665A>G, XM_011540699.3:c.665A>G, XM_011540699.2:c.665A>G, XM_011540699.1:c.665A>G, XP_005245799.1:p.Gln222Arg, NP_689589.1:p.Gln222Arg, XP_011539001.1:p.Gln222Arg

Select item 14835677333.

rs1483567733 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:20190590 (GRCh38)
1:20517083 (GRCh37)
Canonical SPDI:: NC_000001.11:20190589:C:T
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.20190590C>T, NC_000001.10:g.20517083C>T, XM_005245742.5:c.29C>T, XM_005245742.4:c.29C>T, XM_005245742.3:c.29C>T, XM_005245742.2:c.29C>T, XM_005245742.1:c.29C>T, NM_152376.5:c.29C>T, NM_152376.4:c.29C>T, NM_152376.3:c.29C>T, XM_011540699.4:c.29C>T, XM_011540699.3:c.29C>T, XM_011540699.2:c.29C>T, XM_011540699.1:c.29C>T, XP_005245799.1:p.Ala10Val, NP_689589.1:p.Ala10Val, XP_011539001.1:p.Ala10Val

Select item 14819771604.

rs1481977160 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:20191343 (GRCh38)
1:20517836 (GRCh37)
Canonical SPDI:: NC_000001.11:20191342:G:T
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000012/3 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.20191343G>T, NC_000001.10:g.20517836G>T, XM_005245742.5:c.782G>T, XM_005245742.4:c.782G>T, XM_005245742.3:c.782G>T, XM_005245742.2:c.782G>T, XM_005245742.1:c.782G>T, NM_152376.5:c.782G>T, NM_152376.4:c.782G>T, NM_152376.3:c.782G>T, XM_011540699.4:c.782G>T, XM_011540699.3:c.782G>T, XM_011540699.2:c.782G>T, XM_011540699.1:c.782G>T, XP_005245799.1:p.Cys261Phe, NP_689589.1:p.Cys261Phe, XP_011539001.1:p.Cys261Phe

Select item 14788346355.

rs1478834635 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:20190780 (GRCh38)
1:20517273 (GRCh37)
Canonical SPDI:: NC_000001.11:20190779:G:A
Gene:: UBXN10 (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_000001.11:g.20190780G>A, NC_000001.10:g.20517273G>A, XM_005245742.5:c.219G>A, XM_005245742.4:c.219G>A, XM_005245742.3:c.219G>A, XM_005245742.2:c.219G>A, XM_005245742.1:c.219G>A, NM_152376.5:c.219G>A, NM_152376.4:c.219G>A, NM_152376.3:c.219G>A, XM_011540699.4:c.219G>A, XM_011540699.3:c.219G>A, XM_011540699.2:c.219G>A, XM_011540699.1:c.219G>A

Select item 14770188036.

rs1477018803 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:20191107 (GRCh38)
1:20517600 (GRCh37)
Canonical SPDI:: NC_000001.11:20191106:C:G
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.20191107C>G, NC_000001.10:g.20517600C>G, XM_005245742.5:c.546C>G, XM_005245742.4:c.546C>G, XM_005245742.3:c.546C>G, XM_005245742.2:c.546C>G, XM_005245742.1:c.546C>G, NM_152376.5:c.546C>G, NM_152376.4:c.546C>G, NM_152376.3:c.546C>G, XM_011540699.4:c.546C>G, XM_011540699.3:c.546C>G, XM_011540699.2:c.546C>G, XM_011540699.1:c.546C>G

Select item 14661236187.

rs1466123618 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:20191038 (GRCh38)
1:20517531 (GRCh37)
Canonical SPDI:: NC_000001.11:20191037:T:C
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.20191038T>C, NC_000001.10:g.20517531T>C, XM_005245742.5:c.477T>C, XM_005245742.4:c.477T>C, XM_005245742.3:c.477T>C, XM_005245742.2:c.477T>C, XM_005245742.1:c.477T>C, NM_152376.5:c.477T>C, NM_152376.4:c.477T>C, NM_152376.3:c.477T>C, XM_011540699.4:c.477T>C, XM_011540699.3:c.477T>C, XM_011540699.2:c.477T>C, XM_011540699.1:c.477T>C

Select item 14648889418.

rs1464888941 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:20191086 (GRCh38)
1:20517579 (GRCh37)
Canonical SPDI:: NC_000001.11:20191085:C:T
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.000031/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.20191086C>T, NC_000001.10:g.20517579C>T, XM_005245742.5:c.525C>T, XM_005245742.4:c.525C>T, XM_005245742.3:c.525C>T, XM_005245742.2:c.525C>T, XM_005245742.1:c.525C>T, NM_152376.5:c.525C>T, NM_152376.4:c.525C>T, NM_152376.3:c.525C>T, XM_011540699.4:c.525C>T, XM_011540699.3:c.525C>T, XM_011540699.2:c.525C>T, XM_011540699.1:c.525C>T

Select item 14643040129.

rs1464304012 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 1:20191025 (GRCh38)
1:20517518 (GRCh37)
Canonical SPDI:: NC_000001.11:20191024:CC:C
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: CC=0.000071/1 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.20191026del, NC_000001.10:g.20517519del, XM_005245742.5:c.465del, XM_005245742.4:c.465del, XM_005245742.3:c.465del, XM_005245742.2:c.465del, XM_005245742.1:c.465del, NM_152376.5:c.465del, NM_152376.4:c.465del, NM_152376.3:c.465del, XM_011540699.4:c.465del, XM_011540699.3:c.465del, XM_011540699.2:c.465del, XM_011540699.1:c.465del, XP_005245799.1:p.Thr155_Met156insTer, NP_689589.1:p.Thr155_Met156insTer, XP_011539001.1:p.Thr155_Met156insTer

Select item 145951736110.

rs1459517361 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:20190720 (GRCh38)
1:20517213 (GRCh37)
Canonical SPDI:: NC_000001.11:20190719:C:T
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.20190720C>T, NC_000001.10:g.20517213C>T, XM_005245742.5:c.159C>T, XM_005245742.4:c.159C>T, XM_005245742.3:c.159C>T, XM_005245742.2:c.159C>T, XM_005245742.1:c.159C>T, NM_152376.5:c.159C>T, NM_152376.4:c.159C>T, NM_152376.3:c.159C>T, XM_011540699.4:c.159C>T, XM_011540699.3:c.159C>T, XM_011540699.2:c.159C>T, XM_011540699.1:c.159C>T

Select item 145193473111.

rs1451934731 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:20191035 (GRCh38)
1:20517528 (GRCh37)
Canonical SPDI:: NC_000001.11:20191034:A:G
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.20191035A>G, NC_000001.10:g.20517528A>G, XM_005245742.5:c.474A>G, XM_005245742.4:c.474A>G, XM_005245742.3:c.474A>G, XM_005245742.2:c.474A>G, XM_005245742.1:c.474A>G, NM_152376.5:c.474A>G, NM_152376.4:c.474A>G, NM_152376.3:c.474A>G, XM_011540699.4:c.474A>G, XM_011540699.3:c.474A>G, XM_011540699.2:c.474A>G, XM_011540699.1:c.474A>G

Select item 145085114712.

rs1450851147 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:20190843 (GRCh38)
1:20517336 (GRCh37)
Canonical SPDI:: NC_000001.11:20190842:T:C,NC_000001.11:20190842:T:G
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000016/4 (GnomAD_exomes)
C=0.000029/4 (GnomAD)
HGVS:: NC_000001.11:g.20190843T>C, NC_000001.11:g.20190843T>G, NC_000001.10:g.20517336T>C, NC_000001.10:g.20517336T>G, XM_005245742.5:c.282T>C, XM_005245742.5:c.282T>G, XM_005245742.4:c.282T>C, XM_005245742.4:c.282T>G, XM_005245742.3:c.282T>C, XM_005245742.3:c.282T>G, XM_005245742.2:c.282T>C, XM_005245742.2:c.282T>G, XM_005245742.1:c.282T>C, XM_005245742.1:c.282T>G, NM_152376.5:c.282T>C, NM_152376.5:c.282T>G, NM_152376.4:c.282T>C, NM_152376.4:c.282T>G, NM_152376.3:c.282T>C, NM_152376.3:c.282T>G, XM_011540699.4:c.282T>C, XM_011540699.4:c.282T>G, XM_011540699.3:c.282T>C, XM_011540699.3:c.282T>G, XM_011540699.2:c.282T>C, XM_011540699.2:c.282T>G, XM_011540699.1:c.282T>C, XM_011540699.1:c.282T>G, XP_005245799.1:p.Asp94Glu, NP_689589.1:p.Asp94Glu, XP_011539001.1:p.Asp94Glu

Select item 144645937113.

rs1446459371 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:20190751 (GRCh38)
1:20517244 (GRCh37)
Canonical SPDI:: NC_000001.11:20190750:C:A,NC_000001.11:20190750:C:T
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.20190751C>A, NC_000001.11:g.20190751C>T, NC_000001.10:g.20517244C>A, NC_000001.10:g.20517244C>T, XM_005245742.5:c.190C>A, XM_005245742.5:c.190C>T, XM_005245742.4:c.190C>A, XM_005245742.4:c.190C>T, XM_005245742.3:c.190C>A, XM_005245742.3:c.190C>T, XM_005245742.2:c.190C>A, XM_005245742.2:c.190C>T, XM_005245742.1:c.190C>A, XM_005245742.1:c.190C>T, NM_152376.5:c.190C>A, NM_152376.5:c.190C>T, NM_152376.4:c.190C>A, NM_152376.4:c.190C>T, NM_152376.3:c.190C>A, NM_152376.3:c.190C>T, XM_011540699.4:c.190C>A, XM_011540699.4:c.190C>T, XM_011540699.3:c.190C>A, XM_011540699.3:c.190C>T, XM_011540699.2:c.190C>A, XM_011540699.2:c.190C>T, XM_011540699.1:c.190C>A, XM_011540699.1:c.190C>T, XP_005245799.1:p.Pro64Thr, XP_005245799.1:p.Pro64Ser, NP_689589.1:p.Pro64Thr, NP_689589.1:p.Pro64Ser, XP_011539001.1:p.Pro64Thr, XP_011539001.1:p.Pro64Ser

Select item 144423659814.

rs1444236598 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:20190615 (GRCh38)
1:20517108 (GRCh37)
Canonical SPDI:: NC_000001.11:20190614:C:A
Gene:: UBXN10 (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)
HGVS:: NC_000001.11:g.20190615C>A, NC_000001.10:g.20517108C>A, XM_005245742.5:c.54C>A, XM_005245742.4:c.54C>A, XM_005245742.3:c.54C>A, XM_005245742.2:c.54C>A, XM_005245742.1:c.54C>A, NM_152376.5:c.54C>A, NM_152376.4:c.54C>A, NM_152376.3:c.54C>A, XM_011540699.4:c.54C>A, XM_011540699.3:c.54C>A, XM_011540699.2:c.54C>A, XM_011540699.1:c.54C>A

Select item 144028391015.

rs1440283910 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:20190676 (GRCh38)
1:20517169 (GRCh37)
Canonical SPDI:: NC_000001.11:20190675:C:A
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000001.11:g.20190676C>A, NC_000001.10:g.20517169C>A, XM_005245742.5:c.115C>A, XM_005245742.4:c.115C>A, XM_005245742.3:c.115C>A, XM_005245742.2:c.115C>A, XM_005245742.1:c.115C>A, NM_152376.5:c.115C>A, NM_152376.4:c.115C>A, NM_152376.3:c.115C>A, XM_011540699.4:c.115C>A, XM_011540699.3:c.115C>A, XM_011540699.2:c.115C>A, XM_011540699.1:c.115C>A, XP_005245799.1:p.Pro39Thr, NP_689589.1:p.Pro39Thr, XP_011539001.1:p.Pro39Thr

Select item 143774346116.

rs1437743461 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:20190722 (GRCh38)
1:20517215 (GRCh37)
Canonical SPDI:: NC_000001.11:20190721:A:G
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.20190722A>G, NC_000001.10:g.20517215A>G, XM_005245742.5:c.161A>G, XM_005245742.4:c.161A>G, XM_005245742.3:c.161A>G, XM_005245742.2:c.161A>G, XM_005245742.1:c.161A>G, NM_152376.5:c.161A>G, NM_152376.4:c.161A>G, NM_152376.3:c.161A>G, XM_011540699.4:c.161A>G, XM_011540699.3:c.161A>G, XM_011540699.2:c.161A>G, XM_011540699.1:c.161A>G, XP_005245799.1:p.Gln54Arg, NP_689589.1:p.Gln54Arg, XP_011539001.1:p.Gln54Arg

Select item 143425775517.

rs1434257755 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:20191055 (GRCh38)
1:20517548 (GRCh37)
Canonical SPDI:: NC_000001.11:20191054:C:T
Gene:: UBXN10 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.20191055C>T, NC_000001.10:g.20517548C>T, XM_005245742.5:c.494C>T, XM_005245742.4:c.494C>T, XM_005245742.3:c.494C>T, XM_005245742.2:c.494C>T, XM_005245742.1:c.494C>T, NM_152376.5:c.494C>T, NM_152376.4:c.494C>T, NM_152376.3:c.494C>T, XM_011540699.4:c.494C>T, XM_011540699.3:c.494C>T, XM_011540699.2:c.494C>T, XM_011540699.1:c.494C>T, XP_005245799.1:p.Ala165Val, NP_689589.1:p.Ala165Val, XP_011539001.1:p.Ala165Val

Select item 143166883918.

rs1431668839 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:20190763 (GRCh38)
1:20517256 (GRCh37)
Canonical SPDI:: NC_000001.11:20190762:C:T
Gene:: UBXN10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.20190763C>T, NC_000001.10:g.20517256C>T, XM_005245742.5:c.202C>T, XM_005245742.4:c.202C>T, XM_005245742.3:c.202C>T, XM_005245742.2:c.202C>T, XM_005245742.1:c.202C>T, NM_152376.5:c.202C>T, NM_152376.4:c.202C>T, NM_152376.3:c.202C>T, XM_011540699.4:c.202C>T, XM_011540699.3:c.202C>T, XM_011540699.2:c.202C>T, XM_011540699.1:c.202C>T, XP_005245799.1:p.Pro68Ser, NP_689589.1:p.Pro68Ser, XP_011539001.1:p.Pro68Ser

Select item 143010900919.

rs1430109009 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:20190632 (GRCh38)
1:20517125 (GRCh37)
Canonical SPDI:: NC_000001.11:20190631:G:T
Gene:: UBXN10 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.20190632G>T, NC_000001.10:g.20517125G>T, XM_005245742.5:c.71G>T, XM_005245742.4:c.71G>T, XM_005245742.3:c.71G>T, XM_005245742.2:c.71G>T, XM_005245742.1:c.71G>T, NM_152376.5:c.71G>T, NM_152376.4:c.71G>T, NM_152376.3:c.71G>T, XM_011540699.4:c.71G>T, XM_011540699.3:c.71G>T, XM_011540699.2:c.71G>T, XM_011540699.1:c.71G>T, XP_005245799.1:p.Ser24Ile, NP_689589.1:p.Ser24Ile, XP_011539001.1:p.Ser24Ile

Select item 142945716820.

rs1429457168 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:20190963 (GRCh38)
1:20517456 (GRCh37)
Canonical SPDI:: NC_000001.11:20190962:C:T
Gene:: UBXN10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.20190963C>T, NC_000001.10:g.20517456C>T, XM_005245742.5:c.402C>T, XM_005245742.4:c.402C>T, XM_005245742.3:c.402C>T, XM_005245742.2:c.402C>T, XM_005245742.1:c.402C>T, NM_152376.5:c.402C>T, NM_152376.4:c.402C>T, NM_152376.3:c.402C>T, XM_011540699.4:c.402C>T, XM_011540699.3:c.402C>T, XM_011540699.2:c.402C>T, XM_011540699.1:c.402C>T

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