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TTGACCTTGGACTCAACCCCTTTCC[A/C]CCAGGCCCCTTCCCAGCACCGGTGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607320 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAM98C 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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FAM98C - family with sequence similarity 98 member C | ||||||
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There are no transcripts associated with this gene. |
RASGRP4 - RAS guanyl releasing protein 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001146202.1 | Intron | NP_001139674.1 | ||||
NM_001146203.1 | Intron | NP_001139675.1 | ||||
NM_001146204.1 | Intron | NP_001139676.1 | ||||
NM_001146205.1 | Intron | NP_001139677.1 | ||||
NM_001146206.1 | Intron | NP_001139678.1 | ||||
NM_001146207.1 | Intron | NP_001139679.1 | ||||
NM_170604.2 | Intron | NP_733749.1 |