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TGATTCGCAATCTGCATTCTTCTTC[A/T]TCAATTAATTCACCGACGTATTCAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615003 MIM: 607083 | ||||||||||||||||||||
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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There are no transcripts associated with this gene. |
WHSC1L1 - Wolf-Hirschhorn syndrome candidate 1-like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_017778.2 | 4058 | Intron | NP_060248.2 | |||
NM_023034.1 | 4058 | Missense Mutation | GAA,GAT | E,D 1180 | NP_075447.1 |