SNP Links for Protein (Select 767904498) - SNP

Links from Protein

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Select item 14855222341.

rs1485522234 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:64177843 (GRCh38)
1:64643526 (GRCh37)
Canonical SPDI:: NC_000001.11:64177842:C:G
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.64177843C>G, NC_000001.10:g.64643526C>G, NG_032801.2:g.408825C>G, NM_005012.4:c.1802C>G, NM_005012.3:c.1802C>G, XM_011541526.2:c.1613C>G, XM_011541526.1:c.1613C>G, XM_017001376.2:c.1742C>G, XM_017001376.1:c.1742C>G, XM_017001377.2:c.1613C>G, XM_017001377.1:c.1613C>G, NP_005003.2:p.Ala601Gly, XP_011539828.1:p.Ala538Gly, XP_016856865.1:p.Ala581Gly, XP_016856866.1:p.Ala538Gly

Select item 14852184682.

rs1485218468 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:64177833 (GRCh38)
1:64643516 (GRCh37)
Canonical SPDI:: NC_000001.11:64177832:C:G
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_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.64177833C>G, NC_000001.10:g.64643516C>G, NG_032801.2:g.408815C>G, NM_005012.4:c.1792C>G, NM_005012.3:c.1792C>G, XM_011541526.2:c.1603C>G, XM_011541526.1:c.1603C>G, XM_017001376.2:c.1732C>G, XM_017001376.1:c.1732C>G, XM_017001377.2:c.1603C>G, XM_017001377.1:c.1603C>G, NP_005003.2:p.Gln598Glu, XP_011539828.1:p.Gln535Glu, XP_016856865.1:p.Gln578Glu, XP_016856866.1:p.Gln535Glu

Select item 14846706333.

rs1484670633 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:64178205 (GRCh38)
1:64643888 (GRCh37)
Canonical SPDI:: NC_000001.11:64178204:T:C
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.64178205T>C, NC_000001.10:g.64643888T>C, NG_032801.2:g.409187T>C, NM_005012.4:c.2164T>C, NM_005012.3:c.2164T>C, XM_011541526.2:c.1975T>C, XM_011541526.1:c.1975T>C, XM_017001376.2:c.2104T>C, XM_017001376.1:c.2104T>C, XM_017001377.2:c.1975T>C, XM_017001377.1:c.1975T>C, NP_005003.2:p.Tyr722His, XP_011539828.1:p.Tyr659His, XP_016856865.1:p.Tyr702His, XP_016856866.1:p.Tyr659His

Select item 14760905844.

rs1476090584 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:64178218 (GRCh38)
1:64643901 (GRCh37)
Canonical SPDI:: NC_000001.11:64178217:C:G
Gene:: ROR1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.64178218C>G, NC_000001.10:g.64643901C>G, NG_032801.2:g.409200C>G, NM_005012.4:c.2177C>G, NM_005012.3:c.2177C>G, XM_011541526.2:c.1988C>G, XM_011541526.1:c.1988C>G, XM_017001376.2:c.2117C>G, XM_017001376.1:c.2117C>G, XM_017001377.2:c.1988C>G, XM_017001377.1:c.1988C>G, NP_005003.2:p.Thr726Arg, XP_011539828.1:p.Thr663Arg, XP_016856865.1:p.Thr706Arg, XP_016856866.1:p.Thr663Arg

Select item 14758899015.

rs1475889901 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:64140405 (GRCh38)
1:64606088 (GRCh37)
Canonical SPDI:: NC_000001.11:64140404:A:G
Gene:: ROR1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.00011/2 (TOMMO)
G=0.00068/2 (KOREAN)
HGVS:: NC_000001.11:g.64140405A>G, NC_000001.10:g.64606088A>G, NG_032801.2:g.371387A>G, NM_005012.4:c.907A>G, NM_005012.3:c.907A>G, NM_001083592.2:c.907A>G, NM_001083592.1:c.907A>G, XM_011541526.2:c.718A>G, XM_011541526.1:c.718A>G, XM_017001376.2:c.847A>G, XM_017001376.1:c.847A>G, XM_017001377.2:c.718A>G, XM_017001377.1:c.718A>G, NP_005003.2:p.Met303Val, NP_001077061.1:p.Met303Val, XP_011539828.1:p.Met240Val, XP_016856865.1:p.Met283Val, XP_016856866.1:p.Met240Val

Select item 14757550696.

rs1475755069 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:64178566 (GRCh38)
1:64644249 (GRCh37)
Canonical SPDI:: NC_000001.11:64178565:C:T
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.64178566C>T, NC_000001.10:g.64644249C>T, NG_032801.2:g.409548C>T, NM_005012.4:c.2525C>T, NM_005012.3:c.2525C>T, XM_011541526.2:c.2336C>T, XM_011541526.1:c.2336C>T, XM_017001376.2:c.2465C>T, XM_017001376.1:c.2465C>T, XM_017001377.2:c.2336C>T, XM_017001377.1:c.2336C>T, NP_005003.2:p.Pro842Leu, XP_011539828.1:p.Pro779Leu, XP_016856865.1:p.Pro822Leu, XP_016856866.1:p.Pro779Leu

Select item 14750080607.

rs1475008060 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:64142587 (GRCh38)
1:64608270 (GRCh37)
Canonical SPDI:: NC_000001.11:64142586:G:A,NC_000001.11:64142586:G:C
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.64142587G>A, NC_000001.11:g.64142587G>C, NC_000001.10:g.64608270G>A, NC_000001.10:g.64608270G>C, NG_032801.2:g.373569G>A, NG_032801.2:g.373569G>C, NM_005012.4:c.1111G>A, NM_005012.4:c.1111G>C, NM_005012.3:c.1111G>A, NM_005012.3:c.1111G>C, NM_001083592.2:c.1111G>A, NM_001083592.2:c.1111G>C, NM_001083592.1:c.1111G>A, NM_001083592.1:c.1111G>C, XM_011541526.2:c.922G>A, XM_011541526.2:c.922G>C, XM_011541526.1:c.922G>A, XM_011541526.1:c.922G>C, XM_017001376.2:c.1051G>A, XM_017001376.2:c.1051G>C, XM_017001376.1:c.1051G>A, XM_017001376.1:c.1051G>C, XM_017001377.2:c.922G>A, XM_017001377.2:c.922G>C, XM_017001377.1:c.922G>A, XM_017001377.1:c.922G>C, NP_005003.2:p.Ala371Thr, NP_005003.2:p.Ala371Pro, NP_001077061.1:p.Ala371Thr, NP_001077061.1:p.Ala371Pro, XP_011539828.1:p.Ala308Thr, XP_011539828.1:p.Ala308Pro, XP_016856865.1:p.Ala351Thr, XP_016856865.1:p.Ala351Pro, XP_016856866.1:p.Ala308Thr, XP_016856866.1:p.Ala308Pro

Select item 14729589818.

rs1472958981 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:64049740 (GRCh38)
1:64515412 (GRCh37)
Canonical SPDI:: NC_000001.11:64049739:G:A,NC_000001.11:64049739:G:C
Gene:: ROR1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.64049740G>A, NC_000001.11:g.64049740G>C, NC_000001.10:g.64515412G>A, NC_000001.10:g.64515412G>C, NG_032801.2:g.280722G>A, NG_032801.2:g.280722G>C, NM_005012.4:c.213G>A, NM_005012.4:c.213G>C, NM_005012.3:c.213G>A, NM_005012.3:c.213G>C, NM_001083592.2:c.213G>A, NM_001083592.2:c.213G>C, NM_001083592.1:c.213G>A, NM_001083592.1:c.213G>C, XM_011541526.2:c.24G>A, XM_011541526.2:c.24G>C, XM_011541526.1:c.24G>A, XM_011541526.1:c.24G>C, XM_017001376.2:c.153G>A, XM_017001376.2:c.153G>C, XM_017001376.1:c.153G>A, XM_017001376.1:c.153G>C, XM_017001377.2:c.24G>A, XM_017001377.2:c.24G>C, XM_017001377.1:c.24G>A, XM_017001377.1:c.24G>C

Select item 14728185059.

rs1472818505 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:64159182 (GRCh38)
1:64624865 (GRCh37)
Canonical SPDI:: NC_000001.11:64159181:A:G
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.64159182A>G, NC_000001.10:g.64624865A>G, NG_032801.2:g.390164A>G, NM_005012.4:c.1376A>G, NM_005012.3:c.1376A>G, XM_011541526.2:c.1187A>G, XM_011541526.1:c.1187A>G, XM_017001376.2:c.1316A>G, XM_017001376.1:c.1316A>G, XM_017001377.2:c.1187A>G, XM_017001377.1:c.1187A>G, NP_005003.2:p.Tyr459Cys, XP_011539828.1:p.Tyr396Cys, XP_016856865.1:p.Tyr439Cys, XP_016856866.1:p.Tyr396Cys

Select item 147268292410.

rs1472682924 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:64049928 (GRCh38)
1:64515600 (GRCh37)
Canonical SPDI:: NC_000001.11:64049927:C:T
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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.64049928C>T, NC_000001.10:g.64515600C>T, NG_032801.2:g.280910C>T, NM_005012.4:c.401C>T, NM_005012.3:c.401C>T, NM_001083592.2:c.401C>T, NM_001083592.1:c.401C>T, XM_011541526.2:c.212C>T, XM_011541526.1:c.212C>T, XM_017001376.2:c.341C>T, XM_017001376.1:c.341C>T, XM_017001377.2:c.212C>T, XM_017001377.1:c.212C>T, NP_005003.2:p.Thr134Ile, NP_001077061.1:p.Thr134Ile, XP_011539828.1:p.Thr71Ile, XP_016856865.1:p.Thr114Ile, XP_016856866.1:p.Thr71Ile

Select item 147184334511.

rs1471843345 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:64142612 (GRCh38)
1:64608295 (GRCh37)
Canonical SPDI:: NC_000001.11:64142611:A:G
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.64142612A>G, NC_000001.10:g.64608295A>G, NG_032801.2:g.373594A>G, NM_005012.4:c.1136A>G, NM_005012.3:c.1136A>G, NM_001083592.2:c.1136A>G, NM_001083592.1:c.1136A>G, XM_011541526.2:c.947A>G, XM_011541526.1:c.947A>G, XM_017001376.2:c.1076A>G, XM_017001376.1:c.1076A>G, XM_017001377.2:c.947A>G, XM_017001377.1:c.947A>G, NP_005003.2:p.Glu379Gly, NP_001077061.1:p.Glu379Gly, XP_011539828.1:p.Glu316Gly, XP_016856865.1:p.Glu359Gly, XP_016856866.1:p.Glu316Gly

Select item 147084899112.

rs1470848991 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 1:64178789 (GRCh38)
1:64644472 (GRCh37)
Canonical SPDI:: NC_000001.11:64178788:A:C,NC_000001.11:64178788:A:G
Gene:: ROR1 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.64178789A>C, NC_000001.11:g.64178789A>G, NC_000001.10:g.64644472A>C, NC_000001.10:g.64644472A>G, NG_032801.2:g.409771A>C, NG_032801.2:g.409771A>G, NM_005012.4:c.2748A>C, NM_005012.4:c.2748A>G, NM_005012.3:c.2748A>C, NM_005012.3:c.2748A>G, XM_011541526.2:c.2559A>C, XM_011541526.2:c.2559A>G, XM_011541526.1:c.2559A>C, XM_011541526.1:c.2559A>G, XM_017001376.2:c.2688A>C, XM_017001376.2:c.2688A>G, XM_017001376.1:c.2688A>C, XM_017001376.1:c.2688A>G, XM_017001377.2:c.2559A>C, XM_017001377.2:c.2559A>G, XM_017001377.1:c.2559A>C, XM_017001377.1:c.2559A>G, NP_005003.2:p.Gln916His, XP_011539828.1:p.Gln853His, XP_016856865.1:p.Gln896His, XP_016856866.1:p.Gln853His

Select item 147039632813.

rs1470396328 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:64159019 (GRCh38)
1:64624702 (GRCh37)
Canonical SPDI:: NC_000001.11:64159018:C:T
Gene:: ROR1 (Varview)
Functional Consequence:: synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000043/6 (GnomAD)
HGVS:: NC_000001.11:g.64159019C>T, NC_000001.10:g.64624702C>T, NG_032801.2:g.390001C>T, NM_005012.4:c.1213C>T, NM_005012.3:c.1213C>T, XM_011541526.2:c.1024C>T, XM_011541526.1:c.1024C>T, XM_017001376.2:c.1153C>T, XM_017001376.1:c.1153C>T, XM_017001377.2:c.1024C>T, XM_017001377.1:c.1024C>T

Select item 147021432814.

rs1470214328 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:64178068 (GRCh38)
1:64643751 (GRCh37)
Canonical SPDI:: NC_000001.11:64178067:G:T
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.64178068G>T, NC_000001.10:g.64643751G>T, NG_032801.2:g.409050G>T, NM_005012.4:c.2027G>T, NM_005012.3:c.2027G>T, XM_011541526.2:c.1838G>T, XM_011541526.1:c.1838G>T, XM_017001376.2:c.1967G>T, XM_017001376.1:c.1967G>T, XM_017001377.2:c.1838G>T, XM_017001377.1:c.1838G>T, NP_005003.2:p.Trp676Leu, XP_011539828.1:p.Trp613Leu, XP_016856865.1:p.Trp656Leu, XP_016856866.1:p.Trp613Leu

Select item 146869650015.

rs1468696500 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:64049805 (GRCh38)
1:64515477 (GRCh37)
Canonical SPDI:: NC_000001.11:64049804:A:G
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.64049805A>G, NC_000001.10:g.64515477A>G, NG_032801.2:g.280787A>G, NM_005012.4:c.278A>G, NM_005012.3:c.278A>G, NM_001083592.2:c.278A>G, NM_001083592.1:c.278A>G, XM_011541526.2:c.89A>G, XM_011541526.1:c.89A>G, XM_017001376.2:c.218A>G, XM_017001376.1:c.218A>G, XM_017001377.2:c.89A>G, XM_017001377.1:c.89A>G, NP_005003.2:p.Lys93Arg, NP_001077061.1:p.Lys93Arg, XP_011539828.1:p.Lys30Arg, XP_016856865.1:p.Lys73Arg, XP_016856866.1:p.Lys30Arg

Select item 146849305316.

rs1468493053 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:64178686 (GRCh38)
1:64644369 (GRCh37)
Canonical SPDI:: NC_000001.11:64178685:T:C
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.64178686T>C, NC_000001.10:g.64644369T>C, NG_032801.2:g.409668T>C, NM_005012.4:c.2645T>C, NM_005012.3:c.2645T>C, XM_011541526.2:c.2456T>C, XM_011541526.1:c.2456T>C, XM_017001376.2:c.2585T>C, XM_017001376.1:c.2585T>C, XM_017001377.2:c.2456T>C, XM_017001377.1:c.2456T>C, NP_005003.2:p.Ile882Thr, XP_011539828.1:p.Ile819Thr, XP_016856865.1:p.Ile862Thr, XP_016856866.1:p.Ile819Thr

Select item 146675384217.

rs1466753842 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:64142409 (GRCh38)
1:64608092 (GRCh37)
Canonical SPDI:: NC_000001.11:64142408:C:T
Gene:: ROR1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.64142409C>T, NC_000001.10:g.64608092C>T, NG_032801.2:g.373391C>T, NM_005012.4:c.933C>T, NM_005012.3:c.933C>T, NM_001083592.2:c.933C>T, NM_001083592.1:c.933C>T, XM_011541526.2:c.744C>T, XM_011541526.1:c.744C>T, XM_017001376.2:c.873C>T, XM_017001376.1:c.873C>T, XM_017001377.2:c.744C>T, XM_017001377.1:c.744C>T

Select item 146613252018.

rs1466132520 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:64050703 (GRCh38)
1:64516375 (GRCh37)
Canonical SPDI:: NC_000001.11:64050702:A:G
Gene:: ROR1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00006/15 (GnomAD_exomes)
G=0.000128/34 (TOPMED)
G=0.000193/27 (GnomAD)
HGVS:: NC_000001.11:g.64050703A>G, NC_000001.10:g.64516375A>G, NG_032801.2:g.281685A>G, NM_005012.4:c.469A>G, NM_005012.3:c.469A>G, NM_001083592.2:c.469A>G, NM_001083592.1:c.469A>G, XM_011541526.2:c.280A>G, XM_011541526.1:c.280A>G, XM_017001376.2:c.409A>G, XM_017001376.1:c.409A>G, XM_017001377.2:c.280A>G, XM_017001377.1:c.280A>G, NP_005003.2:p.Ser157Gly, NP_001077061.1:p.Ser157Gly, XP_011539828.1:p.Ser94Gly, XP_016856865.1:p.Ser137Gly, XP_016856866.1:p.Ser94Gly

Select item 146602495519.

rs1466024955 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:64178633 (GRCh38)
1:64644316 (GRCh37)
Canonical SPDI:: NC_000001.11:64178632:C:A
Gene:: ROR1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.64178633C>A, NC_000001.10:g.64644316C>A, NG_032801.2:g.409615C>A, NM_005012.4:c.2592C>A, NM_005012.3:c.2592C>A, XM_011541526.2:c.2403C>A, XM_011541526.1:c.2403C>A, XM_017001376.2:c.2532C>A, XM_017001376.1:c.2532C>A, XM_017001377.2:c.2403C>A, XM_017001377.1:c.2403C>A, NP_005003.2:p.Ser864Arg, XP_011539828.1:p.Ser801Arg, XP_016856865.1:p.Ser844Arg, XP_016856866.1:p.Ser801Arg

Select item 146574712220.

rs1465747122 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:64159064 (GRCh38)
1:64624747 (GRCh37)
Canonical SPDI:: NC_000001.11:64159063:T:C
Gene:: ROR1 (Varview)
Functional Consequence:: coding_sequence_variant,genic_downstream_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.64159064T>C, NC_000001.10:g.64624747T>C, NG_032801.2:g.390046T>C, NM_005012.4:c.1258T>C, NM_005012.3:c.1258T>C, XM_011541526.2:c.1069T>C, XM_011541526.1:c.1069T>C, XM_017001376.2:c.1198T>C, XM_017001376.1:c.1198T>C, XM_017001377.2:c.1069T>C, XM_017001377.1:c.1069T>C

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