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GTCTGACACGGAATCTGACTCAATG[A/C]CCGCCGATGCTGGTCTTCCAAAGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611414 | ||||||||||||||||||||
Literature Links: |
C19orf44 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 |
C19orf44 - chromosome 19 open reading frame 44 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001288834.1 | 520 | Missense Mutation | ACC,CCC | T,P 122 | NP_001275763.1 | |
NM_032207.3 | 520 | Missense Mutation | ACC,CCC | T,P 122 | NP_115583.1 | |
XM_006722920.3 | 520 | Missense Mutation | ACC,CCC | T,P 122 | XP_006722983.1 | |
XM_011528354.2 | 520 | Missense Mutation | ACC,CCC | T,P 122 | XP_011526656.1 | |
XM_017027350.1 | 520 | Missense Mutation | ACC,CCC | T,P 122 | XP_016882839.1 |
CALR3 - calreticulin 3 | ||||||
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There are no transcripts associated with this gene. |