Product Details
- SNP ID
-
rs201521593
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.6:24806446 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- ACAGTCTCGAGGAAATTTGTCCAAT[C/T]GTTCATATGCCAGCCGCCCATCTTC
- Phenotype
-
MIM: 611410
- Polymorphism
- C/T, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
C6orf229
PubMed Links
Gene Details
- Gene
- C6orf229
- Gene Name
- chromosome 6 open reading frame 229
There are no transcripts associated with this gene.
- Gene
- FAM65B
- Gene Name
- family with sequence similarity 65 member B
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_001286445.1 |
3420 |
Missense Mutation |
CAA,CGA |
Q1024R |
NP_001273374.1 |
NM_001286446.1 |
3420 |
Intron |
|
|
NP_001273375.1 |
NM_001286447.1 |
3420 |
Intron |
|
|
NP_001273376.1 |
NM_014722.3 |
3420 |
Missense Mutation |
CAA,CGA |
Q1045R |
NP_055537.2 |
NM_015864.3 |
3420 |
Intron |
|
|
NP_056948.2 |
XM_006715275.2 |
3420 |
Missense Mutation |
CAA,CGA |
Q1029R |
XP_006715338.1 |
XM_006715277.1 |
3420 |
Missense Mutation |
CAA,CGA |
Q995R |
XP_006715340.1 |
XM_006715279.2 |
3420 |
Missense Mutation |
CAA,CGA |
Q995R |
XP_006715342.1 |
XM_006715281.3 |
3420 |
Intron |
|
|
XP_006715344.1 |
XM_011515007.1 |
3420 |
Missense Mutation |
CAA,CGA |
Q1024R |
XP_011513309.1 |
XM_011515008.2 |
3420 |
Missense Mutation |
CAA,CGA |
Q995R |
XP_011513310.1 |
XM_011515009.1 |
3420 |
Missense Mutation |
CAA,CGA |
Q995R |
XP_011513311.1 |
XM_011515010.2 |
3420 |
Missense Mutation |
CAA,CGA |
Q995R |
XP_011513312.1 |
XM_011515012.1 |
3420 |
Missense Mutation |
CAA,CGA |
Q1079R |
XP_011513314.1 |
XM_017011523.1 |
3420 |
Missense Mutation |
CAA,CGA |
Q995R |
XP_016867012.1 |
XM_017011524.1 |
3420 |
Intron |
|
|
XP_016867013.1 |
XM_017011525.1 |
3420 |
Intron |
|
|
XP_016867014.1 |
XM_017011526.1 |
3420 |
Intron |
|
|
XP_016867015.1 |
XM_017011527.1 |
3420 |
Intron |
|
|
XP_016867016.1 |
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