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GGGGTCCTCAGGGATGTAGACAGTG[C/T]TGTTCCCTTCAGGCATCTACAGAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605381 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105371031 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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LOC105371031 - translation initiation factor IF-2-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017022800.1 | 1397 | Intron | XP_016878289.1 |
RHCG - Rh family C glycoprotein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321041.1 | 1397 | Missense Mutation | AAC,AGC | N,S 443 | NP_001307970.1 | |
NM_016321.2 | 1397 | Missense Mutation | AAC,AGC | N,S 443 | NP_057405.1 |