SNP Links for Protein (Select 632794852) - SNP

Links from Protein

Items: 1 to 20 of 404

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Select item 14906987231.

rs1490698723 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:134421687 (GRCh38)
9:137313533 (GRCh37)
Canonical SPDI:: NC_000009.12:134421686:T:A
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134421687T>A, NC_000009.11:g.137313533T>A, NM_002957.6:c.792T>A, NM_002957.5:c.792T>A, NM_002957.4:c.792T>A, NM_001291920.2:c.711T>A, NM_001291920.1:c.711T>A, NM_001291921.2:c.501T>A, NM_001291921.1:c.501T>A

Select item 14904589432.

rs1490458943 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:134401825 (GRCh38)
9:137293671 (GRCh37)
Canonical SPDI:: NC_000009.12:134401824:C:T
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,synonymous_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_000009.12:g.134401825C>T, NC_000009.11:g.137293671C>T, NM_002957.6:c.222C>T, NM_002957.5:c.222C>T, NM_002957.4:c.222C>T, NM_001291920.2:c.141C>T, NM_001291920.1:c.141C>T

Select item 14886008183.

rs1488600818 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:134401763 (GRCh38)
9:137293609 (GRCh37)
Canonical SPDI:: NC_000009.12:134401762:C:T
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134401763C>T, NC_000009.11:g.137293609C>T, NM_002957.6:c.160C>T, NM_002957.5:c.160C>T, NM_002957.4:c.160C>T, NM_001291920.2:c.79C>T, NM_001291920.1:c.79C>T

Select item 14853159514.

rs1485315951 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134409097 (GRCh38)
9:137300943 (GRCh37)
Canonical SPDI:: NC_000009.12:134409096:G:A
Gene:: RXRA (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)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.134409097G>A, NC_000009.11:g.137300943G>A, NM_002957.6:c.588G>A, NM_002957.5:c.588G>A, NM_002957.4:c.588G>A, NM_001291920.2:c.507G>A, NM_001291920.1:c.507G>A, NM_001291921.2:c.297G>A, NM_001291921.1:c.297G>A

Select item 14824742005.

rs1482474200 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:134431944 (GRCh38)
9:137323790 (GRCh37)
Canonical SPDI:: NC_000009.12:134431943:G:A,NC_000009.12:134431943:G:C
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.134431944G>A, NC_000009.12:g.134431944G>C, NC_000009.11:g.137323790G>A, NC_000009.11:g.137323790G>C, NM_002957.6:c.1083G>A, NM_002957.6:c.1083G>C, NM_002957.5:c.1083G>A, NM_002957.5:c.1083G>C, NM_002957.4:c.1083G>A, NM_002957.4:c.1083G>C, NM_001291920.2:c.1002G>A, NM_001291920.2:c.1002G>C, NM_001291920.1:c.1002G>A, NM_001291920.1:c.1002G>C, NM_001291921.2:c.792G>A, NM_001291921.2:c.792G>C, NM_001291921.1:c.792G>A, NM_001291921.1:c.792G>C, NP_002948.1:p.Gln361His, NP_001278849.1:p.Gln334His, NP_001278850.1:p.Gln264His

Select item 14822208986.

rs1482220898 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:134401713 (GRCh38)
9:137293559 (GRCh37)
Canonical SPDI:: NC_000009.12:134401712:T:A
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,missense_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.134401713T>A, NC_000009.11:g.137293559T>A, NM_002957.6:c.110T>A, NM_002957.5:c.110T>A, NM_002957.4:c.110T>A, NM_001291920.2:c.29T>A, NM_001291920.1:c.29T>A, NP_002948.1:p.Leu37Gln, NP_001278849.1:p.Leu10Gln

Select item 14811248797.

rs1481124879 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:134408298 (GRCh38)
9:137300144 (GRCh37)
Canonical SPDI:: NC_000009.12:134408297:A:G
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000009.12:g.134408298A>G, NC_000009.11:g.137300144A>G, NM_002957.6:c.429A>G, NM_002957.5:c.429A>G, NM_002957.4:c.429A>G, NM_001291920.2:c.348A>G, NM_001291920.1:c.348A>G, NM_001291921.2:c.138A>G, NM_001291921.1:c.138A>G

Select item 14778553828.

rs1477855382 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 9:134401724 (GRCh38)
9:137293570 (GRCh37)
Canonical SPDI:: NC_000009.12:134401723:A:C
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134401724A>C, NC_000009.11:g.137293570A>C, NM_002957.6:c.121A>C, NM_002957.5:c.121A>C, NM_002957.4:c.121A>C, NM_001291920.2:c.40A>C, NM_001291920.1:c.40A>C, NP_002948.1:p.Ile41Leu, NP_001278849.1:p.Ile14Leu

Select item 14770308609.

rs1477030860 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:134408214 (GRCh38)
9:137300060 (GRCh37)
Canonical SPDI:: NC_000009.12:134408213:C:T
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000009.12:g.134408214C>T, NC_000009.11:g.137300060C>T, NM_002957.6:c.345C>T, NM_002957.5:c.345C>T, NM_002957.4:c.345C>T, NM_001291920.2:c.264C>T, NM_001291920.1:c.264C>T, NM_001291921.2:c.54C>T, NM_001291921.1:c.54C>T

Select item 147592730010.

rs1475927300 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134421720 (GRCh38)
9:137313566 (GRCh37)
Canonical SPDI:: NC_000009.12:134421719:G:A
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: A=0.00004/1 (TOMMO)
HGVS:: NC_000009.12:g.134421720G>A, NC_000009.11:g.137313566G>A, NM_002957.6:c.825G>A, NM_002957.5:c.825G>A, NM_002957.4:c.825G>A, NM_001291920.2:c.744G>A, NM_001291920.1:c.744G>A, NM_001291921.2:c.534G>A, NM_001291921.1:c.534G>A

Select item 147254678811.

rs1472546788 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:134434104 (GRCh38)
9:137325950 (GRCh37)
Canonical SPDI:: NC_000009.12:134434103:T:C
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134434104T>C, NC_000009.11:g.137325950T>C, NM_002957.6:c.1138T>C, NM_002957.5:c.1138T>C, NM_002957.4:c.1138T>C, NM_001291920.2:c.1057T>C, NM_001291920.1:c.1057T>C, NM_001291921.2:c.847T>C, NM_001291921.1:c.847T>C, NP_002948.1:p.Ser380Pro, NP_001278849.1:p.Ser353Pro, NP_001278850.1:p.Ser283Pro

Select item 146824489012.

rs1468244890 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134436594 (GRCh38)
9:137328440 (GRCh37)
Canonical SPDI:: NC_000009.12:134436593:G:A
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.134436594G>A, NC_000009.11:g.137328440G>A, NM_002957.6:c.1369G>A, NM_002957.5:c.1369G>A, NM_002957.4:c.1369G>A, NM_001291920.2:c.1288G>A, NM_001291920.1:c.1288G>A, NM_001291921.2:c.1078G>A, NM_001291921.1:c.1078G>A, NP_002948.1:p.Ala457Thr, NP_001278849.1:p.Ala430Thr, NP_001278850.1:p.Ala360Thr

Select item 146383550313.

rs1463835503 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134409091 (GRCh38)
9:137300937 (GRCh37)
Canonical SPDI:: NC_000009.12:134409090:G:A
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000009.12:g.134409091G>A, NC_000009.11:g.137300937G>A, NM_002957.6:c.582G>A, NM_002957.5:c.582G>A, NM_002957.4:c.582G>A, NM_001291920.2:c.501G>A, NM_001291920.1:c.501G>A, NM_001291921.2:c.291G>A, NM_001291921.1:c.291G>A

Select item 145929998714.

rs1459299987 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:134436510 (GRCh38)
9:137328356 (GRCh37)
Canonical SPDI:: NC_000009.12:134436509:G:A,NC_000009.12:134436509:G:C
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000009.12:g.134436510G>A, NC_000009.12:g.134436510G>C, NC_000009.11:g.137328356G>A, NC_000009.11:g.137328356G>C, NM_002957.6:c.1285G>A, NM_002957.6:c.1285G>C, NM_002957.5:c.1285G>A, NM_002957.5:c.1285G>C, NM_002957.4:c.1285G>A, NM_002957.4:c.1285G>C, NM_001291920.2:c.1204G>A, NM_001291920.2:c.1204G>C, NM_001291920.1:c.1204G>A, NM_001291920.1:c.1204G>C, NM_001291921.2:c.994G>A, NM_001291921.2:c.994G>C, NM_001291921.1:c.994G>A, NM_001291921.1:c.994G>C, NP_002948.1:p.Gly429Arg, NP_002948.1:p.Gly429Arg, NP_001278849.1:p.Gly402Arg, NP_001278849.1:p.Gly402Arg, NP_001278850.1:p.Gly332Arg, NP_001278850.1:p.Gly332Arg

Select item 145803723315.

rs1458037233 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:134429186 (GRCh38)
9:137321032 (GRCh37)
Canonical SPDI:: NC_000009.12:134429185:T:C
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134429186T>C, NC_000009.11:g.137321032T>C, NM_002957.6:c.989T>C, NM_002957.5:c.989T>C, NM_002957.4:c.989T>C, NM_001291920.2:c.908T>C, NM_001291920.1:c.908T>C, NM_001291921.2:c.698T>C, NM_001291921.1:c.698T>C, NP_002948.1:p.Leu330Pro, NP_001278849.1:p.Leu303Pro, NP_001278850.1:p.Leu233Pro

Select item 145619870416.

rs1456198704 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:134401832 (GRCh38)
9:137293678 (GRCh37)
Canonical SPDI:: NC_000009.12:134401831:A:T
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134401832A>T, NC_000009.11:g.137293678A>T, NM_002957.6:c.229A>T, NM_002957.5:c.229A>T, NM_002957.4:c.229A>T, NM_001291920.2:c.148A>T, NM_001291920.1:c.148A>T, NP_002948.1:p.Met77Leu, NP_001278849.1:p.Met50Leu

Select item 145516701817.

rs1455167018 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:134434106 (GRCh38)
9:137325952 (GRCh37)
Canonical SPDI:: NC_000009.12:134434105:C:T
Gene:: RXRA (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_000009.12:g.134434106C>T, NC_000009.11:g.137325952C>T, NM_002957.6:c.1140C>T, NM_002957.5:c.1140C>T, NM_002957.4:c.1140C>T, NM_001291920.2:c.1059C>T, NM_001291920.1:c.1059C>T, NM_001291921.2:c.849C>T, NM_001291921.1:c.849C>T

Select item 145497252718.

rs1454972527 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134417274 (GRCh38)
9:137309120 (GRCh37)
Canonical SPDI:: NC_000009.12:134417273:G:A
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000009.12:g.134417274G>A, NC_000009.11:g.137309120G>A, NM_002957.6:c.727G>A, NM_002957.5:c.727G>A, NM_002957.4:c.727G>A, NM_001291920.2:c.646G>A, NM_001291920.1:c.646G>A, NM_001291921.2:c.436G>A, NM_001291921.1:c.436G>A, NP_002948.1:p.Glu243Lys, NP_001278849.1:p.Glu216Lys, NP_001278850.1:p.Glu146Lys

Select item 145481664419.

rs1454816644 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 9:134436513 (GRCh38)
9:137328359 (GRCh37)
Canonical SPDI:: NC_000009.12:134436512:C:G
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.134436513C>G, NC_000009.11:g.137328359C>G, NM_002957.6:c.1288C>G, NM_002957.5:c.1288C>G, NM_002957.4:c.1288C>G, NM_001291920.2:c.1207C>G, NM_001291920.1:c.1207C>G, NM_001291921.2:c.997C>G, NM_001291921.1:c.997C>G, NP_002948.1:p.Leu430Val, NP_001278849.1:p.Leu403Val, NP_001278850.1:p.Leu333Val

Select item 144800326320.

rs1448003263 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:134408194 (GRCh38)
9:137300040 (GRCh37)
Canonical SPDI:: NC_000009.12:134408193:C:A
Gene:: RXRA (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000009.12:g.134408194C>A, NC_000009.11:g.137300040C>A, NM_002957.6:c.325C>A, NM_002957.5:c.325C>A, NM_002957.4:c.325C>A, NM_001291920.2:c.244C>A, NM_001291920.1:c.244C>A, NM_001291921.2:c.34C>A, NM_001291921.1:c.34C>A, NP_002948.1:p.Pro109Thr, NP_001278849.1:p.Pro82Thr, NP_001278850.1:p.Pro12Thr

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