Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTGGATTTAAGTTTAGATTTTTCAA[A/G]GTCTAGAAATTCAGGACACTGATGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607030 MIM: 608169 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
GCA 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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GCA - grancalcin | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_005246446.2 | 3486 | Intron | XP_005246503.1 | |||
XM_006712398.3 | 3486 | Intron | XP_006712461.1 | |||
XM_006712400.3 | 3486 | Intron | XP_006712463.1 | |||
XM_006712401.3 | 3486 | Intron | XP_006712464.1 | |||
XM_011510926.2 | 3486 | Intron | XP_011509228.1 | |||
XM_011510927.2 | 3486 | Intron | XP_011509229.1 | |||
XM_011510928.2 | 3486 | Intron | XP_011509230.1 | |||
XM_017003764.1 | 3486 | Intron | XP_016859253.1 | |||
XM_017003765.1 | 3486 | Intron | XP_016859254.1 | |||
XM_017003766.1 | 3486 | Intron | XP_016859255.1 | |||
XM_017003767.1 | 3486 | Intron | XP_016859256.1 | |||
XM_017003768.1 | 3486 | Intron | XP_016859257.1 | |||
XM_017003769.1 | 3486 | Intron | XP_016859258.1 |
KCNH7 - potassium voltage-gated channel subfamily H member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033272.3 | 3486 | Missense Mutation | CTT,TTT | L,F 1115 | NP_150375.2 | |
NM_173162.2 | 3486 | Intron | NP_775185.1 | |||
XM_011512109.2 | 3486 | Missense Mutation | CTT,TTT | L,F 1123 | XP_011510411.1 | |
XM_017005218.1 | 3486 | Missense Mutation | CTT,TTT | L,F 1120 | XP_016860707.1 | |
XM_017005219.1 | 3486 | Missense Mutation | CTT,TTT | L,F 1112 | XP_016860708.1 | |
XM_017005220.1 | 3486 | Missense Mutation | CTT,TTT | L,F 1108 | XP_016860709.1 | |
XM_017005221.1 | 3486 | Intron | XP_016860710.1 |