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GCCGCTCTTGCCTTCTGCTCACAAG[A/G]TTTCATAGCCAGGACGGGGACCGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 130410 MIM: 154045 MIM: 606008 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CLDND2 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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CLDND2 - claudin domain containing 2 | ||||||
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There are no transcripts associated with this gene. |
ETFB - electron transfer flavoprotein beta subunit | ||||||
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There are no transcripts associated with this gene. |
LIM2 - lens intrinsic membrane protein 2 | ||||||
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There are no transcripts associated with this gene. |
NKG7 - natural killer cell granule protein 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_005601.3 | 497 | Missense Mutation | ACC,ATC | T,I 164 | NP_005592.1 | |
XM_005258955.3 | 497 | Missense Mutation | ACC,ATC | T,I 129 | XP_005259012.1 | |
XM_006723228.3 | 497 | Missense Mutation | ACC,ATC | T,I 115 | XP_006723291.1 |