Product Details

SNP ID
rs148194001
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:119126995 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GAAAGGAGAATCTGTGGCTACAGTG[C/T]GAGTGGGGGTCCTGCTCCTTTGTGT
Phenotype
MIM: 607099
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
C2CD2L PubMed Links

Gene Details

Gene
C2CD2L
Gene Name
C2CD2 like
There are no transcripts associated with this gene.

Gene
HINFP
Gene Name
histone H4 transcription factor
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001243259.1 233 Silent Mutation TGC,TGT C17C NP_001230188.1
NM_015517.4 233 Silent Mutation TGC,TGT C17C NP_056332.2
NM_198971.2 233 Silent Mutation TGC,TGT C17C NP_945322.1
XM_011542744.2 233 Silent Mutation TGC,TGT C31C XP_011541046.1
XM_011542745.2 233 Silent Mutation TGC,TGT C17C XP_011541047.1
XM_011542746.1 233 Intron XP_011541048.1
XM_017017499.1 233 Silent Mutation TGC,TGT C31C XP_016872988.1
XM_017017500.1 233 Silent Mutation TGC,TGT C17C XP_016872989.1
XM_017017501.1 233 Silent Mutation TGC,TGT C17C XP_016872990.1
XM_017017502.1 233 UTR 5 XP_016872991.1
XM_017017503.1 233 UTR 5 XP_016872992.1
XM_017017504.1 233 UTR 5 XP_016872993.1
XM_017017505.1 233 UTR 5 XP_016872994.1
XM_017017506.1 233 UTR 5 XP_016872995.1
XM_017017507.1 233 UTR 5 XP_016872996.1
XM_017017508.1 233 UTR 5 XP_016872997.1
XM_017017509.1 233 Intron XP_016872998.1

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