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CTCCTCCAGTCTGTGTGGTAGAAGT[A/G]ATCTGCATAGCTTACGATGCTGAAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610858 MIM: 605399 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C14orf166 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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C14orf166 - chromosome 14 open reading frame 166 | ||||||
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There are no transcripts associated with this gene. |
NID2 - nidogen 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_007361.3 | 4213 | Missense Mutation | CAC,TAC | H,Y 1327 | NP_031387.3 | |
XM_005267405.4 | 4213 | Missense Mutation | CAC,TAC | H,Y 1354 | XP_005267462.1 | |
XM_005267406.4 | 4213 | Missense Mutation | CAC,TAC | H,Y 1306 | XP_005267463.1 | |
XM_005267407.4 | 4213 | Missense Mutation | CAC,TAC | H,Y 1279 | XP_005267464.1 |