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GTATTCAAACGTGGTTTCTGTGGCT[A/G]AGAGAGTGGTATCCAAGGTTATGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606092 MIM: 601807 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNAJC14 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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DNAJC14 - DnaJ heat shock protein family (Hsp40) member C14 | ||||||
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There are no transcripts associated with this gene. |
MMP19 - matrix metallopeptidase 19 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272101.1 | 1392 | UTR 3 | NP_001259030.1 | |||
NM_002429.5 | 1392 | Missense Mutation | TCA,TTA | S,L 500 | NP_002420.1 | |
XM_006719401.3 | 1392 | Missense Mutation | TCA,TTA | S,L 271 | XP_006719464.1 | |
XM_011538359.1 | 1392 | Missense Mutation | TCA,TTA | S,L 418 | XP_011536661.1 | |
XM_017019308.1 | 1392 | Intron | XP_016874797.1 | |||
XM_017019309.1 | 1392 | Intron | XP_016874798.1 |
TMEM198B - transmembrane protein 198B (pseudogene) | ||||||
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There are no transcripts associated with this gene. |