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- SNP ID:
- rs112682759
- Gene
-
DDHD2PLPP5WHSC1L1 - Gene Name
- Set Membership:
- -
- Chromosome Location:
- Chr.8: 38270411 - 38270411 on Build GRCh38
- Polymorphism:
- C/T, Transition substitution
- Context Sequence [VIC/FAM]:
AATGGGTACAAATGAGTTTCTCATA[C/T]CAATTCCAAATATACACATACCCTT
Genomic Map
Back To TopAssay Details
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 615003
MIM: 610626
MIM: 607083
|
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Literature Links: |
DDHD2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
| 1000Genome | Applied Biosystems® | HapMap | |||
|---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
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AMR
|
| DDHD2 - DDHD domain containing 2 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001164232.1 | Intron | NP_001157704.1 | ||||
| NM_001164234.1 | Intron | NP_001157706.1 | ||||
| NM_015214.2 | Intron | NP_056029.2 | ||||
| XM_005273454.2 | Intron | XP_005273511.1 | ||||
| XM_005273455.3 | Intron | XP_005273512.1 | ||||
| XM_005273456.3 | Intron | XP_005273513.1 | ||||
| XM_011544456.1 | Intron | XP_011542758.1 | ||||
| XM_017013252.1 | Intron | XP_016868741.1 | ||||
| XM_017013253.1 | Intron | XP_016868742.1 | ||||
| XM_017013254.1 | Intron | XP_016868743.1 | ||||
| XM_017013255.1 | Intron | XP_016868744.1 | ||||
| XM_017013256.1 | Intron | XP_016868745.1 | ||||
| PLPP5 - phospholipid phosphatase 5 | ||||||
|---|---|---|---|---|---|---|
| Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
| NM_001102559.1 | Intron | NP_001096029.1 | ||||
| NM_001102560.1 | Intron | NP_001096030.1 | ||||
| NM_032483.3 | Intron | NP_115872.2 | ||||
| XM_005273661.4 | Intron | XP_005273718.2 | ||||
| XM_005273663.3 | Intron | XP_005273720.2 | ||||
| XM_011544670.2 | Intron | XP_011542972.1 | ||||
| XM_011544671.1 | Intron | XP_011542973.1 | ||||
| XM_011544672.1 | Intron | XP_011542974.1 | ||||
| XM_011544674.2 | Intron | XP_011542976.1 | ||||
| XM_011544675.2 | Intron | XP_011542977.1 | ||||
| XM_017013905.1 | Intron | XP_016869394.1 | ||||
| XM_017013906.1 | Intron | XP_016869395.1 | ||||
| XM_017013907.1 | Intron | XP_016869396.1 | ||||
| WHSC1L1 - Wolf-Hirschhorn syndrome candidate 1-like 1 | ||||||
|---|---|---|---|---|---|---|
| There are no transcripts associated with this gene. | ||||||
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