Product Details

SNP ID
rs140126899
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:119127061 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGTTCTTTGAGCATGTCACTCAGCA[C/T]CTGCAGCAGCACCTGCATGGCTCTG
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_001243259.1 299 Silent Mutation CAC,CAT H39H NP_001230188.1
NM_015517.4 299 Silent Mutation CAC,CAT H39H NP_056332.2
NM_198971.2 299 Silent Mutation CAC,CAT H39H NP_945322.1
XM_011542744.2 299 Silent Mutation CAC,CAT H53H XP_011541046.1
XM_011542745.2 299 Silent Mutation CAC,CAT H39H XP_011541047.1
XM_011542746.1 299 Intron XP_011541048.1
XM_017017499.1 299 Silent Mutation CAC,CAT H53H XP_016872988.1
XM_017017500.1 299 Silent Mutation CAC,CAT H39H XP_016872989.1
XM_017017501.1 299 Silent Mutation CAC,CAT H39H XP_016872990.1
XM_017017502.1 299 UTR 5 XP_016872991.1
XM_017017503.1 299 UTR 5 XP_016872992.1
XM_017017504.1 299 UTR 5 XP_016872993.1
XM_017017505.1 299 UTR 5 XP_016872994.1
XM_017017506.1 299 UTR 5 XP_016872995.1
XM_017017507.1 299 UTR 5 XP_016872996.1
XM_017017508.1 299 UTR 5 XP_016872997.1
XM_017017509.1 299 Intron XP_016872998.1

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