Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGCTCACACCACCTTTTTCAACTT[G/T]TTCTGGCGCTGGAACCTAAGTGGAA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601810 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
DNA2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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DNA2 - DNA replication helicase/nuclease 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080449.2 | 2211 | Missense Mutation | AAA,CAA | K,Q 905 | NP_001073918.2 | |
XM_006717680.3 | 2211 | Missense Mutation | AAA,CAA | K,Q 935 | XP_006717743.1 | |
XM_011539417.1 | 2211 | Missense Mutation | AAA,CAA | K,Q 545 | XP_011537719.1 | |
XM_017015799.1 | 2211 | Missense Mutation | AAA,CAA | K,Q 681 | XP_016871288.1 |