Product Details

SNP ID

rs757508152

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:71712772 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTTCTGCAGAGCAGCTATGAGGCC[A/G]GCGTCCCTGAGGACATCCCTGAAGG

Phenotype

MIM: 605516

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C10orf105 PubMed Links

Gene Details

Gene

C10orf105

Gene Name

chromosome 10 open reading frame 105

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001164375.2	3766	UTR 3			NP_001157847.1
NM_001168390.1	3766	UTR 3			NP_001161862.1
XM_011539808.2	3766	UTR 3			XP_011538110.1
XM_011539809.2	3766	UTR 3			XP_011538111.1

Gene

CDH23

Gene Name

cadherin-related 23

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001171930.1	3766	Missense Mutation	AGC,GGC	S1110G	NP_001165401.1
NM_001171931.1	3766	Intron			NP_001165402.1
NM_001171932.1	3766	Intron			NP_001165403.1
NM_001171933.1	3766	Intron			NP_001165404.1
NM_001171934.1	3766	Intron			NP_001165405.1
NM_001171935.1	3766	Intron			NP_001165406.1
NM_001171936.1	3766	Intron			NP_001165407.1
NM_022124.5	3766	Missense Mutation	AGC,GGC	S1110G	NP_071407.4
NM_052836.3	3766	Intron			NP_443068.1
XM_006717940.3	3766	Missense Mutation	AGC,GGC	S1175G	XP_006718003.1
XM_006717942.3	3766	Missense Mutation	AGC,GGC	S1153G	XP_006718005.1
XM_011540039.2	3766	Missense Mutation	AGC,GGC	S1175G	XP_011538341.1
XM_011540042.2	3766	Missense Mutation	AGC,GGC	S1175G	XP_011538344.1
XM_011540043.2	3766	Missense Mutation	AGC,GGC	S1175G	XP_011538345.1
XM_011540044.2	3766	Missense Mutation	AGC,GGC	S1130G	XP_011538346.1
XM_011540045.2	3766	Missense Mutation	AGC,GGC	S1175G	XP_011538347.1
XM_011540046.2	3766	Missense Mutation	AGC,GGC	S995G	XP_011538348.1
XM_011540047.2	3766	Missense Mutation	AGC,GGC	S781G	XP_011538349.1
XM_011540048.2	3766	Missense Mutation	AGC,GGC	S1175G	XP_011538350.1
XM_011540049.2	3766	Missense Mutation	AGC,GGC	S1175G	XP_011538351.1
XM_011540051.2	3766	Missense Mutation	AGC,GGC	S1175G	XP_011538353.1
XM_011540052.2	3766	Intron			XP_011538354.1
XM_017016499.1	3766	Missense Mutation	AGC,GGC	S1155G	XP_016871988.1
XM_017016500.1	3766	Missense Mutation	AGC,GGC	S1175G	XP_016871989.1
XM_017016501.1	3766	Missense Mutation	AGC,GGC	S321G	XP_016871990.1
XM_017016502.1	3766	Missense Mutation	AGC,GGC	S321G	XP_016871991.1
XM_017016503.1	3766	Intron			XP_016871992.1
XM_017016504.1	3766	Intron			XP_016871993.1
XM_017016505.1	3766	Intron			XP_016871994.1
XM_017016506.1	3766	Intron			XP_016871995.1
XM_017016507.1	3766	Intron			XP_016871996.1
XM_017016508.1	3766	Intron			XP_016871997.1

View Full Product Details