Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCTCACACTCACGTTTCCTCCTCAT[C/G]GCGTTCTTCTTTTTCTCCCTGGCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MCF2L2 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 |
MCF2L2 - MCF.2 cell line derived transforming sequence-like 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015078.3 | 2937 | Missense Mutation | CAT,GAT | H,D 1070 | NP_055893.3 | |
XM_011512585.2 | 2937 | Missense Mutation | CAT,GAT | H,D 717 | XP_011510887.1 | |
XM_011512586.2 | 2937 | Missense Mutation | CAT,GAT | H,D 717 | XP_011510888.1 | |
XM_017005943.1 | 2937 | Intron | XP_016861432.1 | |||
XM_017005944.1 | 2937 | Intron | XP_016861433.1 | |||
XM_017005945.1 | 2937 | Intron | XP_016861434.1 | |||
XM_017005946.1 | 2937 | Intron | XP_016861435.1 |