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AGTTAAGGGCTCATTTCTGTTGGGA[A/G]AATACCCTAGAAATGAAAGAAATGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607963 MIM: 606154 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MBD3L1 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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MBD3L1 - methyl-CpG binding domain protein 3 like 1 | ||||||
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There are no transcripts associated with this gene. |
MUC16 - mucin 16, cell surface associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024690.2 | 33381 | Missense Mutation | TCT,TTT | S,F 14437 | NP_078966.2 | |
XM_017027486.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14187 | XP_016882975.1 | |
XM_017027487.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14165 | XP_016882976.1 | |
XM_017027488.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14158 | XP_016882977.1 | |
XM_017027489.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14147 | XP_016882978.1 | |
XM_017027490.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14032 | XP_016882979.1 | |
XM_017027491.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14032 | XP_016882980.1 | |
XM_017027492.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14031 | XP_016882981.1 | |
XM_017027493.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14031 | XP_016882982.1 | |
XM_017027494.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14031 | XP_016882983.1 | |
XM_017027495.1 | 33381 | Missense Mutation | TCT,TTT | S,F 14031 | XP_016882984.1 | |
XM_017027496.1 | 33381 | Missense Mutation | TCT,TTT | S,F 13564 | XP_016882985.1 | |
XM_017027497.1 | 33381 | Missense Mutation | TCT,TTT | S,F 13406 | XP_016882986.1 | |
XM_017027498.1 | 33381 | Intron | XP_016882987.1 | |||
XM_017027499.1 | 33381 | Missense Mutation | TCT,TTT | S,F 11116 | XP_016882988.1 | |
XM_017027500.1 | 33381 | Missense Mutation | TCT,TTT | S,F 11089 | XP_016882989.1 | |
XM_017027501.1 | 33381 | Missense Mutation | TCT,TTT | S,F 1745 | XP_016882990.1 |