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CTAAGGATCTCATCTGGACTTTGTT[A/T]TTCCTGGGAACTGCAGGTACATTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 116930 | ||||||||||||||||||||
Literature Links: |
LOC101928847 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 |
LOC101928847 - uncharacterized LOC101928847 | ||||||
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There are no transcripts associated with this gene. |
NCAM1 - neural cell adhesion molecule 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000615.6 | 402 | Missense Mutation | TTA,TTT | L,F 12 | NP_000606.3 | |
NM_001076682.3 | 402 | Missense Mutation | TTA,TTT | L,F 12 | NP_001070150.1 | |
NM_001242607.1 | 402 | Missense Mutation | TTA,TTT | L,F 12 | NP_001229536.1 | |
NM_001242608.1 | 402 | Missense Mutation | TTA,TTT | L,F 12 | NP_001229537.1 | |
NM_181351.4 | 402 | Missense Mutation | TTA,TTT | L,F 12 | NP_851996.2 |