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CTGGTTCTGTCATTGCTCAGCCTAG[C/T]TGGCGTCCAGCTTGGCCATTTCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 610054 | ||||||||||||||||||||
Literature Links: |
C5orf66 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 |
C5orf66 - chromosome 5 open reading frame 66 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277348.1 | 1325 | Intron | NP_001264277.1 |
H2AFY - H2A histone family member Y | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040158.1 | 1325 | Missense Mutation | AAC,AGC | N,S 371 | NP_001035248.1 | |
NM_004893.2 | 1325 | Missense Mutation | AAC,AGC | N,S 371 | NP_004884.1 | |
NM_138609.2 | 1325 | Missense Mutation | AAC,AGC | N,S 369 | NP_613075.1 | |
NM_138610.2 | 1325 | Missense Mutation | AAC,AGC | N,S 372 | NP_613258.2 | |
XM_005272132.1 | 1325 | Missense Mutation | AAC,AGC | N,S 368 | XP_005272189.1 | |
XM_005272134.3 | 1325 | Intron | XP_005272191.1 | |||
XM_005272135.3 | 1325 | Intron | XP_005272192.1 | |||
XM_011543729.2 | 1325 | Missense Mutation | AAC,AGC | N,S 372 | XP_011542031.1 | |
XM_011543730.2 | 1325 | Missense Mutation | AAC,AGC | N,S 371 | XP_011542032.1 | |
XM_011543731.1 | 1325 | UTR 3 | XP_011542033.1 | |||
XM_011543732.1 | 1325 | UTR 3 | XP_011542034.1 | |||
XM_011543733.2 | 1325 | Intron | XP_011542035.1 | |||
XM_011543734.2 | 1325 | Intron | XP_011542036.1 | |||
XM_011543735.2 | 1325 | Intron | XP_011542037.1 | |||
XM_017010067.1 | 1325 | UTR 3 | XP_016865556.1 | |||
XM_017010068.1 | 1325 | Intron | XP_016865557.1 | |||
XM_017010069.1 | 1325 | Intron | XP_016865558.1 |