Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCCCATTAGAGAAAATGTCTTGGG[A/G]ATAAGTTTCTGGGGCAGCGTGATCC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MAP7D2 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 |
MAP7D2 - MAP7 domain containing 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168465.1 | 1840 | Missense Mutation | CCC,TCC | P,S 651 | NP_001161937.1 | |
NM_001168466.1 | 1840 | Missense Mutation | CCC,TCC | P,S 565 | NP_001161938.1 | |
NM_001168467.1 | 1840 | Missense Mutation | CCC,TCC | P,S 558 | NP_001161939.1 | |
NM_152780.3 | 1840 | Missense Mutation | CCC,TCC | P,S 610 | NP_689993.2 | |
XM_005274478.2 | 1840 | Missense Mutation | CCC,TCC | P,S 635 | XP_005274535.1 | |
XM_005274479.2 | 1840 | Missense Mutation | CCC,TCC | P,S 624 | XP_005274536.1 | |
XM_005274480.3 | 1840 | Missense Mutation | CCC,TCC | P,S 602 | XP_005274537.1 | |
XM_006724481.2 | 1840 | Missense Mutation | CCC,TCC | P,S 684 | XP_006724544.1 | |
XM_006724482.2 | 1840 | Missense Mutation | CCC,TCC | P,S 643 | XP_006724545.1 | |
XM_011545483.1 | 1840 | Missense Mutation | CCC,TCC | P,S 673 | XP_011543785.1 | |
XM_011545484.1 | 1840 | Missense Mutation | CCC,TCC | P,S 640 | XP_011543786.1 | |
XM_011545485.1 | 1840 | Missense Mutation | CCC,TCC | P,S 629 | XP_011543787.1 | |
XM_011545486.2 | 1840 | Intron | XP_011543788.1 | |||
XM_017029393.1 | 1840 | Missense Mutation | CCC,TCC | P,S 632 | XP_016884882.1 | |
XM_017029394.1 | 1840 | Missense Mutation | CCC,TCC | P,S 599 | XP_016884883.1 | |
XM_017029395.1 | 1840 | Missense Mutation | CCC,TCC | P,S 591 | XP_016884884.1 | |
XM_017029396.1 | 1840 | Missense Mutation | CCC,TCC | P,S 588 | XP_016884885.1 | |
XM_017029397.1 | 1840 | Missense Mutation | CCC,TCC | P,S 580 | XP_016884886.1 | |
XM_017029398.1 | 1840 | Intron | XP_016884887.1 |
MIR23C - microRNA 23c | ||||||
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There are no transcripts associated with this gene. |