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CTCATTCTGGGACGTGGTGGGGATG[A/G]AGGTATGGGTCACATCCTGCTCTAT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 611429 | |||||||||||||||||||||||
Literature Links: |
C3orf35 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
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 |
C3orf35 - chromosome 3 open reading frame 35 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001302831.1 | 4569 | Intron | NP_001289760.1 | |||
NM_001302832.1 | 4569 | Intron | NP_001289761.1 | |||
NM_178339.2 | 4569 | Intron | NP_848029.2 | |||
NM_178342.2 | 4569 | Intron | NP_848032.1 | |||
NM_178344.2 | 4569 | Intron | NP_848034.2 | |||
XM_017006291.1 | 4569 | Intron | XP_016861780.1 | |||
XM_017006292.1 | 4569 | Intron | XP_016861781.1 | |||
XM_017006293.1 | 4569 | UTR 5 | XP_016861782.1 | |||
XM_017006294.1 | 4569 | Intron | XP_016861783.1 | |||
XM_017006295.1 | 4569 | Intron | XP_016861784.1 | |||
XM_017006296.1 | 4569 | Intron | XP_016861785.1 |