Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCGGCGGGGGCTACACCAACCGGA[C/T]CTTCGAGTTTGACGACGGCCAATGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608167 MIM: 610224 | ||||||||||||||||||||
Literature Links: |
KCNT1 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 |
KCNT1 - potassium sodium-activated channel subfamily T member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001272003.1 | 1529 | Missense Mutation | ACC,ATC | T,I 26 | NP_001258932.1 | |
NM_020822.2 | 1529 | Missense Mutation | ACC,ATC | T,I 26 | NP_065873.2 | |
XM_011518877.2 | 1529 | UTR 5 | XP_011517179.1 | |||
XM_011518878.2 | 1529 | UTR 5 | XP_011517180.1 | |||
XM_011518879.2 | 1529 | UTR 5 | XP_011517181.1 | |||
XM_011518880.1 | 1529 | Intron | XP_011517182.1 | |||
XM_011518881.2 | 1529 | Intron | XP_011517183.1 | |||
XM_017014931.1 | 1529 | Intron | XP_016870420.1 | |||
XM_017014932.1 | 1529 | Intron | XP_016870421.1 | |||
XM_017014933.1 | 1529 | Intron | XP_016870422.1 |
SOHLH1 - spermatogenesis and oogenesis specific basic helix-loop-helix 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001012415.2 | 1529 | Intron | NP_001012415.2 | |||
NM_001101677.1 | 1529 | Intron | NP_001095147.1 |