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TGCTGCCCCGAACTCTCCTAGGCCC[A/G]TCGCCCCATTTCCTGCAACAGCCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607762 MIM: 602716 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
KIRREL2 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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KIRREL2 - kin of IRRE like 2 (Drosophila) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032123.6 | 338 | Silent Mutation | CCA,CCG | P,P 22 | NP_115499.5 | |
NM_199179.3 | 338 | Intron | NP_954648.3 | |||
NM_199180.3 | 338 | Silent Mutation | CCA,CCG | P,P 22 | NP_954649.3 | |
XM_011527362.1 | 338 | Silent Mutation | CCA,CCG | P,P 22 | XP_011525664.1 | |
XM_011527363.1 | 338 | Silent Mutation | CCA,CCG | P,P 22 | XP_011525665.1 | |
XM_011527365.1 | 338 | Intron | XP_011525667.1 | |||
XM_011527366.1 | 338 | Intron | XP_011525668.1 | |||
XM_017027348.1 | 338 | Silent Mutation | CCA,CCG | P,P 22 | XP_016882837.1 |
NPHS1 - NPHS1, nephrin | ||||||
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There are no transcripts associated with this gene. |