SNP Links for Protein (Select 71774083) - SNP - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Links from Protein

Items: 1 to 20 of 455

<< First< Prev

Page of 23

Select item 14906444421.

rs1490644442 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:127738287 (GRCh38)
8:128750533 (GRCh37)
Canonical SPDI:: NC_000008.11:127738286:A:T
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.127738287A>T, NC_000008.10:g.128750533A>T, NG_007161.2:g.7854A>T, NM_002467.6:c.70A>T, NM_002467.5:c.70A>T, NM_002467.4:c.70A>T, NM_001354870.1:c.67A>T, NP_002458.2:p.Asn24Tyr, NP_001341799.1:p.Asn23Tyr

Select item 14900579412.

rs1490057941 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:127740546 (GRCh38)
8:128752792 (GRCh37)
Canonical SPDI:: NC_000008.11:127740545:C:G
Gene:: MYC (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_000008.11:g.127740546C>G, NC_000008.10:g.128752792C>G, NG_007161.2:g.10113C>G, NM_002467.6:c.953C>G, NM_002467.5:c.953C>G, NM_002467.4:c.953C>G, NM_001354870.1:c.950C>G, NP_002458.2:p.Ser318Cys, NP_001341799.1:p.Ser317Cys

Select item 14894208103.

rs1489420810 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:127738945 (GRCh38)
8:128751191 (GRCh37)
Canonical SPDI:: NC_000008.11:127738944:A:T
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.127738945A>T, NC_000008.10:g.128751191A>T, NG_007161.2:g.8512A>T, NM_002467.6:c.728A>T, NM_002467.5:c.728A>T, NM_002467.4:c.728A>T, NM_001354870.1:c.725A>T, NP_002458.2:p.Glu243Val, NP_001341799.1:p.Glu242Val

Select item 14875612084.

rs1487561208 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 8:127740908 (GRCh38)
8:128753154 (GRCh37)
Canonical SPDI:: NC_000008.11:127740907:C:A,NC_000008.11:127740907:C:G,NC_000008.11:127740907:C:T
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,stop_gained,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.127740908C>A, NC_000008.11:g.127740908C>G, NC_000008.11:g.127740908C>T, NC_000008.10:g.128753154C>A, NC_000008.10:g.128753154C>G, NC_000008.10:g.128753154C>T, NG_007161.2:g.10475C>A, NG_007161.2:g.10475C>G, NG_007161.2:g.10475C>T, NM_002467.6:c.1315C>A, NM_002467.6:c.1315C>G, NM_002467.6:c.1315C>T, NM_002467.5:c.1315C>A, NM_002467.5:c.1315C>G, NM_002467.5:c.1315C>T, NM_002467.4:c.1315C>A, NM_002467.4:c.1315C>G, NM_002467.4:c.1315C>T, NM_001354870.1:c.1312C>A, NM_001354870.1:c.1312C>G, NM_001354870.1:c.1312C>T, NP_002458.2:p.Arg439Gly, NP_002458.2:p.Arg439Ter, NP_001341799.1:p.Arg438Gly, NP_001341799.1:p.Arg438Ter

Select item 14843857455.

rs1484385745 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 8:127738467 (GRCh38)
8:128750713 (GRCh37)
Canonical SPDI:: NC_000008.11:127738466:C:A,NC_000008.11:127738466:C:G,NC_000008.11:127738466:C:T
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.127738467C>A, NC_000008.11:g.127738467C>G, NC_000008.11:g.127738467C>T, NC_000008.10:g.128750713C>A, NC_000008.10:g.128750713C>G, NC_000008.10:g.128750713C>T, NG_007161.2:g.8034C>A, NG_007161.2:g.8034C>G, NG_007161.2:g.8034C>T, NM_002467.6:c.250C>A, NM_002467.6:c.250C>G, NM_002467.6:c.250C>T, NM_002467.5:c.250C>A, NM_002467.5:c.250C>G, NM_002467.5:c.250C>T, NM_002467.4:c.250C>A, NM_002467.4:c.250C>G, NM_002467.4:c.250C>T, NM_001354870.1:c.247C>A, NM_001354870.1:c.247C>G, NM_001354870.1:c.247C>T, NP_002458.2:p.Leu84Ile, NP_002458.2:p.Leu84Val, NP_002458.2:p.Leu84Phe, NP_001341799.1:p.Leu83Ile, NP_001341799.1:p.Leu83Val, NP_001341799.1:p.Leu83Phe

Select item 14803671436.

rs1480367143 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:127740669 (GRCh38)
8:128752915 (GRCh37)
Canonical SPDI:: NC_000008.11:127740668:G:A
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.127740669G>A, NC_000008.10:g.128752915G>A, NG_007161.2:g.10236G>A, NM_002467.6:c.1076G>A, NM_002467.5:c.1076G>A, NM_002467.4:c.1076G>A, NM_001354870.1:c.1073G>A, NP_002458.2:p.Ser359Asn, NP_001341799.1:p.Ser358Asn

Select item 14794191017.

rs1479419101 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 8:127740596 (GRCh38)
8:128752842 (GRCh37)
Canonical SPDI:: NC_000008.11:127740595:C:A,NC_000008.11:127740595:C:G
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.127740596C>A, NC_000008.11:g.127740596C>G, NC_000008.10:g.128752842C>A, NC_000008.10:g.128752842C>G, NG_007161.2:g.10163C>A, NG_007161.2:g.10163C>G, NM_002467.6:c.1003C>A, NM_002467.6:c.1003C>G, NM_002467.5:c.1003C>A, NM_002467.5:c.1003C>G, NM_002467.4:c.1003C>A, NM_002467.4:c.1003C>G, NM_001354870.1:c.1000C>A, NM_001354870.1:c.1000C>G, NP_002458.2:p.Pro335Thr, NP_002458.2:p.Pro335Ala, NP_001341799.1:p.Pro334Thr, NP_001341799.1:p.Pro334Ala

Select item 14791815508.

rs1479181550 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:127740850 (GRCh38)
8:128753096 (GRCh37)
Canonical SPDI:: NC_000008.11:127740849:G:A
Gene:: MYC (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=0.000021/3 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000008.11:g.127740850G>A, NC_000008.10:g.128753096G>A, NG_007161.2:g.10417G>A, NM_002467.6:c.1257G>A, NM_002467.5:c.1257G>A, NM_002467.4:c.1257G>A, NM_001354870.1:c.1254G>A

Select item 14789218989.

rs1478921898 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 8:127738620 (GRCh38)
8:128750866 (GRCh37)
Canonical SPDI:: NC_000008.11:127738619:G:A,NC_000008.11:127738619:G:C,NC_000008.11:127738619:G:T
Gene:: MYC (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_000008.11:g.127738620G>A, NC_000008.11:g.127738620G>C, NC_000008.11:g.127738620G>T, NC_000008.10:g.128750866G>A, NC_000008.10:g.128750866G>C, NC_000008.10:g.128750866G>T, NG_007161.2:g.8187G>A, NG_007161.2:g.8187G>C, NG_007161.2:g.8187G>T, NM_002467.6:c.403G>A, NM_002467.6:c.403G>C, NM_002467.6:c.403G>T, NM_002467.5:c.403G>A, NM_002467.5:c.403G>C, NM_002467.5:c.403G>T, NM_002467.4:c.403G>A, NM_002467.4:c.403G>C, NM_002467.4:c.403G>T, NM_001354870.1:c.400G>A, NM_001354870.1:c.400G>C, NM_001354870.1:c.400G>T, NP_002458.2:p.Asp135Asn, NP_002458.2:p.Asp135His, NP_002458.2:p.Asp135Tyr, NP_001341799.1:p.Asp134Asn, NP_001341799.1:p.Asp134His, NP_001341799.1:p.Asp134Tyr

Select item 147849912710.

rs1478499127 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:127740936 (GRCh38)
8:128753182 (GRCh37)
Canonical SPDI:: NC_000008.11:127740935:A:G
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.127740936A>G, NC_000008.10:g.128753182A>G, NG_007161.2:g.10503A>G, NM_002467.6:c.1343A>G, NM_002467.5:c.1343A>G, NM_002467.4:c.1343A>G, NM_001354870.1:c.1340A>G, NP_002458.2:p.Gln448Arg, NP_001341799.1:p.Gln447Arg

Select item 147645536111.

rs1476455361 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 8:127738905 (GRCh38)
8:128751151 (GRCh37)
Canonical SPDI:: NC_000008.11:127738904:G:A,NC_000008.11:127738904:G:C
Gene:: MYC (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_000008.11:g.127738905G>A, NC_000008.11:g.127738905G>C, NC_000008.10:g.128751151G>A, NC_000008.10:g.128751151G>C, NG_007161.2:g.8472G>A, NG_007161.2:g.8472G>C, NM_002467.6:c.688G>A, NM_002467.6:c.688G>C, NM_002467.5:c.688G>A, NM_002467.5:c.688G>C, NM_002467.4:c.688G>A, NM_002467.4:c.688G>C, NM_001354870.1:c.685G>A, NM_001354870.1:c.685G>C, NP_002458.2:p.Ala230Thr, NP_002458.2:p.Ala230Pro, NP_001341799.1:p.Ala229Thr, NP_001341799.1:p.Ala229Pro

Select item 147467949912.

rs1474679499 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 8:127738815 (GRCh38)
8:128751061 (GRCh37)
Canonical SPDI:: NC_000008.11:127738814:G:A,NC_000008.11:127738814:G:C
Gene:: MYC (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.127738815G>A, NC_000008.11:g.127738815G>C, NC_000008.10:g.128751061G>A, NC_000008.10:g.128751061G>C, NG_007161.2:g.8382G>A, NG_007161.2:g.8382G>C, NM_002467.6:c.598G>A, NM_002467.6:c.598G>C, NM_002467.5:c.598G>A, NM_002467.5:c.598G>C, NM_002467.4:c.598G>A, NM_002467.4:c.598G>C, NM_001354870.1:c.595G>A, NM_001354870.1:c.595G>C, NP_002458.2:p.Ala200Thr, NP_002458.2:p.Ala200Pro, NP_001341799.1:p.Ala199Thr, NP_001341799.1:p.Ala199Pro

Select item 146907507913.

rs1469075079 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 8:127738780 (GRCh38)
8:128751026 (GRCh37)
Canonical SPDI:: NC_000008.11:127738779:C:G,NC_000008.11:127738779:C:T
Gene:: MYC (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_000008.11:g.127738780C>G, NC_000008.11:g.127738780C>T, NC_000008.10:g.128751026C>G, NC_000008.10:g.128751026C>T, NG_007161.2:g.8347C>G, NG_007161.2:g.8347C>T, NM_002467.6:c.563C>G, NM_002467.6:c.563C>T, NM_002467.5:c.563C>G, NM_002467.5:c.563C>T, NM_002467.4:c.563C>G, NM_002467.4:c.563C>T, NM_001354870.1:c.560C>G, NM_001354870.1:c.560C>T, NP_002458.2:p.Thr188Ser, NP_002458.2:p.Thr188Ile, NP_001341799.1:p.Thr187Ser, NP_001341799.1:p.Thr187Ile

Select item 146904959514.

rs1469049595 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 8:127738487 (GRCh38)
8:128750733 (GRCh37)
Canonical SPDI:: NC_000008.11:127738486:T:A,NC_000008.11:127738486:T:C
Gene:: MYC (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.127738487T>A, NC_000008.11:g.127738487T>C, NC_000008.10:g.128750733T>A, NC_000008.10:g.128750733T>C, NG_007161.2:g.8054T>A, NG_007161.2:g.8054T>C, NM_002467.6:c.270T>A, NM_002467.6:c.270T>C, NM_002467.5:c.270T>A, NM_002467.5:c.270T>C, NM_002467.4:c.270T>A, NM_002467.4:c.270T>C, NM_001354870.1:c.267T>A, NM_001354870.1:c.267T>C

Select item 146840863015.

rs1468408630 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:127738672 (GRCh38)
8:128750918 (GRCh37)
Canonical SPDI:: NC_000008.11:127738671:G:C
Gene:: MYC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.127738672G>C, NC_000008.10:g.128750918G>C, NG_007161.2:g.8239G>C, NM_002467.6:c.455G>C, NM_002467.5:c.455G>C, NM_002467.4:c.455G>C, NM_001354870.1:c.452G>C, NP_002458.2:p.Gly152Ala, NP_001341799.1:p.Gly151Ala

Select item 146749689116.

rs1467496891 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:127738825 (GRCh38)
8:128751071 (GRCh37)
Canonical SPDI:: NC_000008.11:127738824:G:A
Gene:: MYC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000008.11:g.127738825G>A, NC_000008.10:g.128751071G>A, NG_007161.2:g.8392G>A, NM_002467.6:c.608G>A, NM_002467.5:c.608G>A, NM_002467.4:c.608G>A, NM_001354870.1:c.605G>A, NP_002458.2:p.Cys203Tyr, NP_001341799.1:p.Cys202Tyr

Select item 146709582717.

rs1467095827 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 8:127738989 (GRCh38)
8:128751235 (GRCh37)
Canonical SPDI:: NC_000008.11:127738988:G:A,NC_000008.11:127738988:G:C
Gene:: MYC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.127738989G>A, NC_000008.11:g.127738989G>C, NC_000008.10:g.128751235G>A, NC_000008.10:g.128751235G>C, NG_007161.2:g.8556G>A, NG_007161.2:g.8556G>C, NM_002467.6:c.772G>A, NM_002467.6:c.772G>C, NM_002467.5:c.772G>A, NM_002467.5:c.772G>C, NM_002467.4:c.772G>A, NM_002467.4:c.772G>C, NM_001354870.1:c.769G>A, NM_001354870.1:c.769G>C, NP_002458.2:p.Glu258Lys, NP_002458.2:p.Glu258Gln, NP_001341799.1:p.Glu257Lys, NP_001341799.1:p.Glu257Gln

Select item 146669614318.

rs1466696143 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 8:127738892 (GRCh38)
8:128751138 (GRCh37)
Canonical SPDI:: NC_000008.11:127738891:G:A,NC_000008.11:127738891:G:C,NC_000008.11:127738891:G:T
Gene:: MYC (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000008.11:g.127738892G>A, NC_000008.11:g.127738892G>C, NC_000008.11:g.127738892G>T, NC_000008.10:g.128751138G>A, NC_000008.10:g.128751138G>C, NC_000008.10:g.128751138G>T, NG_007161.2:g.8459G>A, NG_007161.2:g.8459G>C, NG_007161.2:g.8459G>T, NM_002467.6:c.675G>A, NM_002467.6:c.675G>C, NM_002467.6:c.675G>T, NM_002467.5:c.675G>A, NM_002467.5:c.675G>C, NM_002467.5:c.675G>T, NM_002467.4:c.675G>A, NM_002467.4:c.675G>C, NM_002467.4:c.675G>T, NM_001354870.1:c.672G>A, NM_001354870.1:c.672G>C, NM_001354870.1:c.672G>T

Select item 146517375019.

rs1465173750 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:127740906 (GRCh38)
8:128753152 (GRCh37)
Canonical SPDI:: NC_000008.11:127740905:G:A
Gene:: MYC (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.127740906G>A, NC_000008.10:g.128753152G>A, NG_007161.2:g.10473G>A, NM_002467.6:c.1313G>A, NM_002467.5:c.1313G>A, NM_002467.4:c.1313G>A, NM_001354870.1:c.1310G>A, NP_002458.2:p.Arg438Gln, NP_001341799.1:p.Arg437Gln

Select item 146153072520.

rs1461530725 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 8:127738808 (GRCh38)
8:128751054 (GRCh37)
Canonical SPDI:: NC_000008.11:127738807:C:A,NC_000008.11:127738807:C:G,NC_000008.11:127738807:C:T
Gene:: MYC (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.127738808C>A, NC_000008.11:g.127738808C>G, NC_000008.11:g.127738808C>T, NC_000008.10:g.128751054C>A, NC_000008.10:g.128751054C>G, NC_000008.10:g.128751054C>T, NG_007161.2:g.8375C>A, NG_007161.2:g.8375C>G, NG_007161.2:g.8375C>T, NM_002467.6:c.591C>A, NM_002467.6:c.591C>G, NM_002467.6:c.591C>T, NM_002467.5:c.591C>A, NM_002467.5:c.591C>G, NM_002467.5:c.591C>T, NM_002467.4:c.591C>A, NM_002467.4:c.591C>G, NM_002467.4:c.591C>T, NM_001354870.1:c.588C>A, NM_001354870.1:c.588C>G, NM_001354870.1:c.588C>T, NP_002458.2:p.Ser197Arg, NP_002458.2:p.Ser197Arg, NP_001341799.1:p.Ser196Arg, NP_001341799.1:p.Ser196Arg

<< First< Prev

Page of 23

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Protein (Select 71774083) (455)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...