Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAGTCCTCCTGAGAGATTGTTCCTC[A/G]GCCTTCAGGGTCATAATTCTTGAAC
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 |
---|---|---|
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 |
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 | 1559 | Nonsense Mutation | CGA,TGA | R,* 469 | NP_001139674.1 | |
NM_001146203.1 | 1559 | Nonsense Mutation | CGA,TGA | R,* 391 | NP_001139675.1 | |
NM_001146204.1 | 1559 | Nonsense Mutation | CGA,TGA | R,* 414 | NP_001139676.1 | |
NM_001146205.1 | 1559 | Nonsense Mutation | CGA,TGA | R,* 449 | NP_001139677.1 | |
NM_001146206.1 | 1559 | Nonsense Mutation | CGA,TGA | R,* 294 | NP_001139678.1 | |
NM_001146207.1 | 1559 | Nonsense Mutation | CGA,TGA | R,* 386 | NP_001139679.1 | |
NM_170604.2 | 1559 | Nonsense Mutation | CGA,TGA | R,* 483 | NP_733749.1 |