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CTGTTAGAATTGGAGTTCTCGTTGT[C/T]CTCCCTGCAAGTGCGGGAGCAAAGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604994 | ||||||||||||||||||||
Literature Links: |
SIX2 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 |
SIX2 - SIX homeobox 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016932.4 | 858 | Missense Mutation | AAC,GAC | N,D 189 | NP_058628.3 | |
XM_005264100.3 | 858 | Missense Mutation | AAC,GAC | N,D 191 | XP_005264157.1 |