Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCAAAGACTGGAGATCTACCTTCTG[A/C]TTTGATGACTTTTCTGCATTAATCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 612032 | ||||||||||||||||||||
Literature Links: |
DPY30 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 |
DPY30 - dpy-30, histone methyltransferase complex regulatory subunit | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001321209.1 | 273 | Missense Mutation | AAG,AAT | K,N 43 | NP_001308138.1 | |
NM_001321210.1 | 273 | Missense Mutation | AAG,AAT | K,N 43 | NP_001308139.1 | |
NM_032574.3 | 273 | Missense Mutation | AAG,AAT | K,N 43 | NP_115963.1 | |
XM_006712117.3 | 273 | Missense Mutation | AAG,AAT | K,N 43 | XP_006712180.1 | |
XM_006712118.3 | 273 | Intron | XP_006712181.1 | |||
XM_011533133.2 | 273 | Missense Mutation | AAG,AAT | K,N 43 | XP_011531435.1 | |
XM_017005111.1 | 273 | Missense Mutation | AAG,AAT | K,N 43 | XP_016860600.1 |