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CTTGTCCTGTGGGGCTCTGGGCGGC[C/G]GAGGTTGGCGGTCCGGGCCCGCCGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605349 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C17orf62 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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C17orf62 - chromosome 17 open reading frame 62 | ||||||
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There are no transcripts associated with this gene. |
NARF - nuclear prelamin A recognition factor | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001038618.2 | 26 | Intron | NP_001033707.1 | |||
NM_001083608.1 | 26 | Intron | NP_001077077.1 | |||
NM_012336.3 | 26 | Intron | NP_036468.1 | |||
NM_031968.2 | 26 | Intron | NP_114174.1 | |||
XM_005256340.3 | 26 | Intron | XP_005256397.1 | |||
XM_006722278.3 | 26 | Intron | XP_006722341.1 | |||
XM_011523541.2 | 26 | UTR 5 | XP_011521843.1 | |||
XM_011523543.2 | 26 | Intron | XP_011521845.1 | |||
XM_011523544.2 | 26 | Intron | XP_011521846.1 | |||
XM_017024449.1 | 26 | Intron | XP_016879938.1 | |||
XM_017024450.1 | 26 | Intron | XP_016879939.1 |