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CTGGCTGAACCCTTGAAACATGAAA[G/T]CCCAGCCGCTCCCTCAAGTGCTGGC
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 608351 | |||||||||||||||||||||||
Literature Links: |
C3orf30 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 |
C3orf30 - chromosome 3 open reading frame 30 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_152539.2 | 90 | Missense Mutation | AGC,ATC | S,I 17 | NP_689752.2 |
IGSF11 - immunoglobulin superfamily member 11 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001015887.1 | 90 | Intron | NP_001015887.1 | |||
NM_152538.2 | 90 | Intron | NP_689751.2 | |||
XM_006713517.1 | 90 | Intron | XP_006713580.1 | |||
XM_011512462.2 | 90 | Intron | XP_011510764.1 | |||
XM_011512463.1 | 90 | Intron | XP_011510765.1 | |||
XM_011512464.2 | 90 | Intron | XP_011510766.1 | |||
XM_011512465.1 | 90 | Intron | XP_011510767.1 | |||
XM_011512466.2 | 90 | Intron | XP_011510768.1 | |||
XM_011512467.2 | 90 | Intron | XP_011510769.1 | |||
XM_011512468.1 | 90 | Intron | XP_011510770.1 | |||
XM_011512469.1 | 90 | Intron | XP_011510771.1 | |||
XM_011512470.1 | 90 | Intron | XP_011510772.1 | |||
XM_011512471.2 | 90 | Intron | XP_011510773.1 | |||
XM_011512472.1 | 90 | Intron | XP_011510774.1 | |||
XM_011512474.2 | 90 | Intron | XP_011510776.1 | |||
XM_017005789.1 | 90 | Intron | XP_016861278.1 | |||
XM_017005790.1 | 90 | Intron | XP_016861279.1 |