Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142590 MIM: 142580 | ||||||||||||||||||||
Literature Links: |
BAG6 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
BAG6 - BCL2 associated athanogene 6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001098534.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1118 | NP_001092004.1 | |
NM_001199697.1 | 3685 | Missense Mutation | GCC,GGC | A,G 895 | NP_001186626.1 | |
NM_001199698.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1069 | NP_001186627.1 | |
NM_004639.3 | 3685 | Missense Mutation | GCC,GGC | A,G 1124 | NP_004630.3 | |
NM_080702.2 | 3685 | Missense Mutation | GCC,GGC | A,G 1118 | NP_542433.1 | |
NM_080703.2 | 3685 | Missense Mutation | GCC,GGC | A,G 1118 | NP_542434.1 | |
XM_011514892.2 | 3685 | Missense Mutation | GCC,GGC | A,G 1165 | XP_011513194.1 | |
XM_017011275.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866764.1 | |
XM_017011276.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866765.1 | |
XM_017011277.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866766.1 | |
XM_017011278.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866767.1 | |
XM_017011279.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866768.1 | |
XM_017011280.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866769.1 | |
XM_017011281.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866770.1 | |
XM_017011282.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1174 | XP_016866771.1 | |
XM_017011283.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1173 | XP_016866772.1 | |
XM_017011284.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1163 | XP_016866773.1 | |
XM_017011285.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1156 | XP_016866774.1 | |
XM_017011286.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1156 | XP_016866775.1 | |
XM_017011287.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1154 | XP_016866776.1 | |
XM_017011288.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1135 | XP_016866777.1 | |
XM_017011289.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1127 | XP_016866778.1 | |
XM_017011290.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1126 | XP_016866779.1 | |
XM_017011291.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1125 | XP_016866780.1 | |
XM_017011292.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1117 | XP_016866781.1 | |
XM_017011293.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1100 | XP_016866782.1 | |
XM_017011294.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1092 | XP_016866783.1 | |
XM_017011295.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1077 | XP_016866784.1 | |
XM_017011296.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1068 | XP_016866785.1 | |
XM_017011297.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1086 | XP_016866786.1 | |
XM_017011298.1 | 3685 | Missense Mutation | GCC,GGC | A,G 1020 | XP_016866787.1 |
MIR6832 - microRNA 6832 | ||||||
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There are no transcripts associated with this gene. |
PRRC2A - proline rich coiled-coil 2A | ||||||
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There are no transcripts associated with this gene. |