Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GAATGTGAGGTGGGTGAACAGAGAT[C/G]ACCGGGTAGGCTCACTTGTTCTTTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608684 | ||||||||||||||||||||
Literature Links: |
NIN 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 |
NIN - ninein | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016350.4 | 6250 | Missense Mutation | CAT,GAT | H,D 1357 | NP_057434.4 | |
NM_020921.3 | 6250 | Intron | NP_065972.3 | |||
NM_182944.2 | 6250 | Intron | NP_891989.2 | |||
NM_182946.1 | 6250 | Missense Mutation | CAT,GAT | H,D 2070 | NP_891991.1 | |
XM_011536817.1 | 6250 | Intron | XP_011535119.1 | |||
XM_011536819.2 | 6250 | Intron | XP_011535121.1 | |||
XM_011536822.1 | 6250 | Intron | XP_011535124.1 | |||
XM_011536823.2 | 6250 | Missense Mutation | CAT,GAT | H,D 2076 | XP_011535125.1 |