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CTTAGGAGTGCTGGCCTTGAGTTTC[A/G]CAAAAGGCTCCAAATTGGTGAGGTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 614806 | ||||||||||||||||||||
Literature Links: |
DMRTC2 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 |
DMRTC2 - DMRT like family C2 | ||||||
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There are no transcripts associated with this gene. |
LYPD4 - LY6/PLAUR domain containing 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001291419.1 | 618 | Missense Mutation | GCG,GTG | A,V 90 | NP_001278348.1 | |
NM_173506.6 | 618 | Missense Mutation | GCG,GTG | A,V 125 | NP_775777.3 | |
XM_005258543.3 | 618 | Missense Mutation | GCG,GTG | A,V 138 | XP_005258600.1 | |
XM_005278383.4 | 618 | Missense Mutation | GCG,GTG | A,V 138 | XP_005278440.1 | |
XM_005278385.4 | 618 | Missense Mutation | GCG,GTG | A,V 138 | XP_005278442.1 | |
XM_005278387.4 | 618 | Missense Mutation | GCG,GTG | A,V 138 | XP_005278444.1 | |
XM_005278388.3 | 618 | Missense Mutation | GCG,GTG | A,V 76 | XP_005278445.1 | |
XM_006723035.2 | 618 | Missense Mutation | GCG,GTG | A,V 134 | XP_006723098.1 | |
XM_011526483.2 | 618 | Missense Mutation | GCG,GTG | A,V 138 | XP_011524785.1 | |
XM_011526484.2 | 618 | Missense Mutation | GCG,GTG | A,V 138 | XP_011524786.1 |