Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATAAGTATGTTCCCTACTCGGAGAG[C/G]TTCAGCCAAGTTTTAGAGGTATTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615003 | ||||||||||||||||||||
Literature Links: |
DDHD2 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 |
DDHD2 - DDHD domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164232.1 | 918 | Missense Mutation | AGC,AGG | S,R 131 | NP_001157704.1 | |
NM_001164234.1 | 918 | Missense Mutation | AGC,AGG | S,R 131 | NP_001157706.1 | |
NM_015214.2 | 918 | Missense Mutation | AGC,AGG | S,R 131 | NP_056029.2 | |
XM_005273454.2 | 918 | Missense Mutation | AGC,AGG | S,R 131 | XP_005273511.1 | |
XM_005273455.3 | 918 | Missense Mutation | AGC,AGG | S,R 131 | XP_005273512.1 | |
XM_005273456.3 | 918 | Missense Mutation | AGC,AGG | S,R 131 | XP_005273513.1 | |
XM_011544456.1 | 918 | Missense Mutation | AGC,AGG | S,R 131 | XP_011542758.1 | |
XM_017013252.1 | 918 | Missense Mutation | AGC,AGG | S,R 131 | XP_016868741.1 | |
XM_017013253.1 | 918 | Missense Mutation | AGC,AGG | S,R 131 | XP_016868742.1 | |
XM_017013254.1 | 918 | UTR 5 | XP_016868743.1 | |||
XM_017013255.1 | 918 | UTR 5 | XP_016868744.1 | |||
XM_017013256.1 | 918 | UTR 5 | XP_016868745.1 |