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TGAAGTTAATGCTACATCCTCCTCA[G/T]CTCCATCACTGTCTCGGGCTGAAAG
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607437 | ||||||||||||||||||||||||||
Literature Links: |
FAM234B PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese)
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AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR - Not Available | |||||
AMR - Not Available |
FAM234B - family with sequence similarity 234 member B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020853.1 | 3354 | Intron | NP_065904.1 | |||
XM_017019706.1 | 3354 | Intron | XP_016875195.1 |
GPRC5D - G protein-coupled receptor class C group 5 member D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018654.1 | 3354 | Missense Mutation | GAT,GCT | D,A 305 | NP_061124.1 | |
XM_005253421.3 | 3354 | Missense Mutation | GAT,GCT | D,A 305 | XP_005253478.1 | |
XM_017019582.1 | 3354 | Missense Mutation | GAT,GCT | D,A 305 | XP_016875071.1 | |
XM_017019583.1 | 3354 | Intron | XP_016875072.1 |
Set Membership: |
HapMap |