Product Details

SNP ID
rs202079073
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:119127090 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCAGCACCTGCATGGCTCTGGGG[A/T]GGAGGAGGAAGAGGAAGAGGAGGAT
Phenotype
MIM: 607099
Polymorphism
A/T, Transversion 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_001243259.1 328 Missense Mutation GAG,GTG E49V NP_001230188.1
NM_015517.4 328 Missense Mutation GAG,GTG E49V NP_056332.2
NM_198971.2 328 Missense Mutation GAG,GTG E49V NP_945322.1
XM_011542744.2 328 Missense Mutation GAG,GTG E63V XP_011541046.1
XM_011542745.2 328 Missense Mutation GAG,GTG E49V XP_011541047.1
XM_011542746.1 328 Intron XP_011541048.1
XM_017017499.1 328 Missense Mutation GAG,GTG E63V XP_016872988.1
XM_017017500.1 328 Missense Mutation GAG,GTG E49V XP_016872989.1
XM_017017501.1 328 Missense Mutation GAG,GTG E49V XP_016872990.1
XM_017017502.1 328 UTR 5 XP_016872991.1
XM_017017503.1 328 UTR 5 XP_016872992.1
XM_017017504.1 328 UTR 5 XP_016872993.1
XM_017017505.1 328 UTR 5 XP_016872994.1
XM_017017506.1 328 UTR 5 XP_016872995.1
XM_017017507.1 328 UTR 5 XP_016872996.1
XM_017017508.1 328 UTR 5 XP_016872997.1
XM_017017509.1 328 Intron XP_016872998.1

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