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AGGCAGGGCTGGGCCCCTGCCGGCC[A/G]CCCCGGCCCCCTGTGACTCTCTTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601964 MIM: 604497 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNAJC7 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DNAJC7 - DnaJ heat shock protein family (Hsp40) member C7 | ||||||
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There are no transcripts associated with this gene. |
NKIRAS2 - NFKB inhibitor interacting Ras like 2 | ||||||
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There are no transcripts associated with this gene. |
ZNF385C - zinc finger protein 385C | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001242704.1 | 1779 | Silent Mutation | GGC,GGT | G,G 283 | NP_001229633.1 | |
XM_006721751.3 | 1779 | Silent Mutation | GGC,GGT | G,G 230 | XP_006721814.1 | |
XM_011524475.2 | 1779 | Intron | XP_011522777.1 | |||
XM_011524476.1 | 1779 | Intron | XP_011522778.1 | |||
XM_011524477.2 | 1779 | Intron | XP_011522779.1 | |||
XM_011524478.2 | 1779 | Intron | XP_011522780.1 | |||
XM_011524479.2 | 1779 | Silent Mutation | GGC,GGT | G,G 363 | XP_011522781.1 | |
XM_011524482.2 | 1779 | Silent Mutation | GGC,GGT | G,G 362 | XP_011522784.1 | |
XM_011524483.2 | 1779 | Silent Mutation | GGC,GGT | G,G 363 | XP_011522785.1 | |
XM_017024314.1 | 1779 | Silent Mutation | GGC,GGT | G,G 405 | XP_016879803.1 | |
XM_017024315.1 | 1779 | Silent Mutation | GGC,GGT | G,G 405 | XP_016879804.1 | |
XM_017024316.1 | 1779 | Silent Mutation | GGC,GGT | G,G 404 | XP_016879805.1 | |
XM_017024317.1 | 1779 | Silent Mutation | GGC,GGT | G,G 405 | XP_016879806.1 | |
XM_017024318.1 | 1779 | Silent Mutation | GGC,GGT | G,G 404 | XP_016879807.1 | |
XM_017024319.1 | 1779 | Silent Mutation | GGC,GGT | G,G 362 | XP_016879808.1 | |
XM_017024320.1 | 1779 | Silent Mutation | GGC,GGT | G,G 272 | XP_016879809.1 | |
XM_017024321.1 | 1779 | Intron | XP_016879810.1 |