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TCTGCAGAGCAGCTATGAGGCCAGC[G/T]TCCCTGAGGACATCCCTGAAGGCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605516 | ||||||||||||||||||||
Literature Links: |
C10orf105 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 |
C10orf105 - chromosome 10 open reading frame 105 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164375.2 | 3763 | UTR 3 | NP_001157847.1 | |||
NM_001168390.1 | 3763 | UTR 3 | NP_001161862.1 | |||
XM_011539808.2 | 3763 | UTR 3 | XP_011538110.1 | |||
XM_011539809.2 | 3763 | UTR 3 | XP_011538111.1 |
CDH23 - cadherin-related 23 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171930.1 | 3763 | Missense Mutation | GTC,TTC | V,F 1111 | NP_001165401.1 | |
NM_001171931.1 | 3763 | Intron | NP_001165402.1 | |||
NM_001171932.1 | 3763 | Intron | NP_001165403.1 | |||
NM_001171933.1 | 3763 | Intron | NP_001165404.1 | |||
NM_001171934.1 | 3763 | Intron | NP_001165405.1 | |||
NM_001171935.1 | 3763 | Intron | NP_001165406.1 | |||
NM_001171936.1 | 3763 | Intron | NP_001165407.1 | |||
NM_022124.5 | 3763 | Missense Mutation | GTC,TTC | V,F 1111 | NP_071407.4 | |
NM_052836.3 | 3763 | Intron | NP_443068.1 | |||
XM_006717940.3 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_006718003.1 | |
XM_006717942.3 | 3763 | Missense Mutation | GTC,TTC | V,F 1154 | XP_006718005.1 | |
XM_011540039.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_011538341.1 | |
XM_011540042.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_011538344.1 | |
XM_011540043.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_011538345.1 | |
XM_011540044.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1131 | XP_011538346.1 | |
XM_011540045.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_011538347.1 | |
XM_011540046.2 | 3763 | Missense Mutation | GTC,TTC | V,F 996 | XP_011538348.1 | |
XM_011540047.2 | 3763 | Missense Mutation | GTC,TTC | V,F 782 | XP_011538349.1 | |
XM_011540048.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_011538350.1 | |
XM_011540049.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_011538351.1 | |
XM_011540051.2 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_011538353.1 | |
XM_011540052.2 | 3763 | Intron | XP_011538354.1 | |||
XM_017016499.1 | 3763 | Missense Mutation | GTC,TTC | V,F 1156 | XP_016871988.1 | |
XM_017016500.1 | 3763 | Missense Mutation | GTC,TTC | V,F 1176 | XP_016871989.1 | |
XM_017016501.1 | 3763 | Missense Mutation | GTC,TTC | V,F 322 | XP_016871990.1 | |
XM_017016502.1 | 3763 | Missense Mutation | GTC,TTC | V,F 322 | XP_016871991.1 | |
XM_017016503.1 | 3763 | Intron | XP_016871992.1 | |||
XM_017016504.1 | 3763 | Intron | XP_016871993.1 | |||
XM_017016505.1 | 3763 | Intron | XP_016871994.1 | |||
XM_017016506.1 | 3763 | Intron | XP_016871995.1 | |||
XM_017016507.1 | 3763 | Intron | XP_016871996.1 | |||
XM_017016508.1 | 3763 | Intron | XP_016871997.1 |