Product Details
- SNP ID
-
rs145207671
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:31639154 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- AGCTAAGGATCATCAGCAAAGGCCC[A/G]CTGGGCATTGGGGAAGCGCTGGGGA
- Phenotype
-
MIM: 142590
MIM: 142580
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
BAG6
PubMed Links
Gene Details
- Gene
- BAG6
- Gene Name
- BCL2 associated athanogene 6
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001098534.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1120W |
NP_001092004.1 |
NM_001199697.1 |
3690 |
Missense Mutation |
CGG,TGG |
R897W |
NP_001186626.1 |
NM_001199698.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1071W |
NP_001186627.1 |
NM_004639.3 |
3690 |
Missense Mutation |
CGG,TGG |
R1126W |
NP_004630.3 |
NM_080702.2 |
3690 |
Missense Mutation |
CGG,TGG |
R1120W |
NP_542433.1 |
NM_080703.2 |
3690 |
Missense Mutation |
CGG,TGG |
R1120W |
NP_542434.1 |
XM_011514892.2 |
3690 |
Missense Mutation |
CGG,TGG |
R1167W |
XP_011513194.1 |
XM_017011275.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866764.1 |
XM_017011276.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866765.1 |
XM_017011277.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866766.1 |
XM_017011278.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866767.1 |
XM_017011279.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866768.1 |
XM_017011280.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866769.1 |
XM_017011281.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866770.1 |
XM_017011282.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1176W |
XP_016866771.1 |
XM_017011283.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1175W |
XP_016866772.1 |
XM_017011284.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1165W |
XP_016866773.1 |
XM_017011285.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1158W |
XP_016866774.1 |
XM_017011286.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1158W |
XP_016866775.1 |
XM_017011287.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1156W |
XP_016866776.1 |
XM_017011288.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1137W |
XP_016866777.1 |
XM_017011289.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1129W |
XP_016866778.1 |
XM_017011290.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1128W |
XP_016866779.1 |
XM_017011291.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1127W |
XP_016866780.1 |
XM_017011292.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1119W |
XP_016866781.1 |
XM_017011293.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1102W |
XP_016866782.1 |
XM_017011294.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1094W |
XP_016866783.1 |
XM_017011295.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1079W |
XP_016866784.1 |
XM_017011296.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1070W |
XP_016866785.1 |
XM_017011297.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1088W |
XP_016866786.1 |
XM_017011298.1 |
3690 |
Missense Mutation |
CGG,TGG |
R1022W |
XP_016866787.1 |
- Gene
- MIR6832
- Gene Name
- microRNA 6832
There are no transcripts associated with this gene.
- Gene
- PRRC2A
- Gene Name
- proline rich coiled-coil 2A
There are no transcripts associated with this gene.
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