Product Details
- SNP ID
-
rs199981422
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.17:28758321 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- GAAGACTTCGACTCTCTGTGGGATC[A/G]GGGGCTCGGTTGCCAGGGGCTCGGT
- Phenotype
-
MIM: 602464
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
FAM222B
PubMed Links
Gene Details
- Gene
- FAM222B
- Gene Name
- family with sequence similarity 222 member B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001077498.2 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
NP_001070966.1 |
NM_001288631.1 |
2007 |
Silent Mutation |
CCC,CCT |
P548P |
NP_001275560.1 |
NM_001288632.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
NP_001275561.1 |
NM_001288633.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
NP_001275562.1 |
NM_001288634.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
NP_001275563.1 |
NM_001288635.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
NP_001275564.1 |
NM_001288636.1 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
NP_001275565.1 |
NM_001288637.1 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
NP_001275566.1 |
NM_001288638.1 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
NP_001275567.1 |
NM_001288639.1 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
NP_001275568.1 |
NM_001288640.1 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
NP_001275569.1 |
NM_018182.3 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
NP_060652.2 |
XM_011524986.2 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
XP_011523288.1 |
XM_011524987.1 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
XP_011523289.1 |
XM_011524988.2 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
XP_011523290.1 |
XM_017024831.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
XP_016880320.1 |
XM_017024832.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
XP_016880321.1 |
XM_017024833.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
XP_016880322.1 |
XM_017024834.1 |
2007 |
Silent Mutation |
CCC,CCT |
P546P |
XP_016880323.1 |
XM_017024835.1 |
2007 |
Silent Mutation |
CCC,CCT |
P418P |
XP_016880324.1 |
- Gene
- TRAF4
- Gene Name
- TNF receptor associated factor 4
There are no transcripts associated with this gene.
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