Product Details

SNP ID
rs142924253
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:119127113 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGAGGAGGAGGAAGAGGAAGAGGAG[A/G]ATGACCCACTTGGTAAGAGAGCAGG
Phenotype
MIM: 607099
Polymorphism
A/G, 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_001243259.1 351 Missense Mutation AAT,GAT N57D NP_001230188.1
NM_015517.4 351 Missense Mutation AAT,GAT N57D NP_056332.2
NM_198971.2 351 Missense Mutation AAT,GAT N57D NP_945322.1
XM_011542744.2 351 Missense Mutation AAT,GAT N71D XP_011541046.1
XM_011542745.2 351 Missense Mutation AAT,GAT N57D XP_011541047.1
XM_011542746.1 351 Intron XP_011541048.1
XM_017017499.1 351 Missense Mutation AAT,GAT N71D XP_016872988.1
XM_017017500.1 351 Missense Mutation AAT,GAT N57D XP_016872989.1
XM_017017501.1 351 Missense Mutation AAT,GAT N57D XP_016872990.1
XM_017017502.1 351 UTR 5 XP_016872991.1
XM_017017503.1 351 UTR 5 XP_016872992.1
XM_017017504.1 351 UTR 5 XP_016872993.1
XM_017017505.1 351 UTR 5 XP_016872994.1
XM_017017506.1 351 UTR 5 XP_016872995.1
XM_017017507.1 351 UTR 5 XP_016872996.1
XM_017017508.1 351 UTR 5 XP_016872997.1
XM_017017509.1 351 Intron XP_016872998.1

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