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AGTCATGCCTGCCTGAGACGCCCCG[C/T]GGTTGGTGCCCATCTGTAACCCGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
16 submissions
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Phenotype: |
MIM: 609738 MIM: 604634 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
IGSF9 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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IGSF9 - immunoglobulin superfamily member 9 | ||||||
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There are no transcripts associated with this gene. |
TAGLN2 - transgelin 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001277223.1 | 855 | Intron | NP_001264152.1 | |||
NM_001277224.1 | 855 | Missense Mutation | CAC,CGC | H,R 203 | NP_001264153.1 | |
NM_003564.2 | 855 | Intron | NP_003555.1 |