Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608441 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
SYNE1 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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SYNE1 - spectrin repeat containing nuclear envelope protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_033071.3 | 26669 | Missense Mutation | AGC,GGC | S,G 8689 | NP_149062.1 | |
NM_182961.3 | 26669 | Missense Mutation | AGC,GGC | S,G 8737 | NP_892006.3 | |
XM_006715407.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8786 | XP_006715470.1 | |
XM_006715408.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8782 | XP_006715471.1 | |
XM_006715409.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8779 | XP_006715472.1 | |
XM_006715410.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8772 | XP_006715473.1 | |
XM_006715411.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8769 | XP_006715474.1 | |
XM_006715412.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8767 | XP_006715475.1 | |
XM_006715413.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8763 | XP_006715476.1 | |
XM_006715414.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8762 | XP_006715477.1 | |
XM_006715415.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8749 | XP_006715478.1 | |
XM_006715416.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8744 | XP_006715479.1 | |
XM_006715417.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8739 | XP_006715480.1 | |
XM_006715420.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8735 | XP_006715483.1 | |
XM_006715421.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8734 | XP_006715484.1 | |
XM_006715422.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8733 | XP_006715485.1 | |
XM_006715423.2 | 26669 | UTR 3 | XP_006715486.1 | |||
XM_006715424.2 | 26669 | UTR 3 | XP_006715487.1 | |||
XM_006715425.2 | 26669 | UTR 3 | XP_006715488.1 | |||
XM_011535641.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8785 | XP_011533943.1 | |
XM_011535642.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8781 | XP_011533944.1 | |
XM_011535643.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8731 | XP_011533945.1 | |
XM_011535644.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8211 | XP_011533946.1 | |
XM_011535645.2 | 26669 | Missense Mutation | AGC,GGC | S,G 8042 | XP_011533947.1 | |
XM_017010608.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8786 | XP_016866097.1 | |
XM_017010609.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8786 | XP_016866098.1 | |
XM_017010610.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8779 | XP_016866099.1 | |
XM_017010611.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8777 | XP_016866100.1 | |
XM_017010612.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8760 | XP_016866101.1 | |
XM_017010613.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8748 | XP_016866102.1 | |
XM_017010614.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8734 | XP_016866103.1 | |
XM_017010615.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8697 | XP_016866104.1 | |
XM_017010616.1 | 26669 | UTR 3 | XP_016866105.1 | |||
XM_017010617.1 | 26669 | UTR 3 | XP_016866106.1 | |||
XM_017010618.1 | 26669 | UTR 3 | XP_016866107.1 | |||
XM_017010619.1 | 26669 | Missense Mutation | AGC,GGC | S,G 8211 | XP_016866108.1 |