Product Details

SNP ID

rs202101019

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.10:71712674 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTTCAACTCCCACAGACAACGGCC[C/T]TGTAGGGAAGCGACACACGGGCACA

Phenotype

MIM: 605516

Polymorphism

C/T, 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	3864	UTR 3			NP_001157847.1
NM_001168390.1	3864	UTR 3			NP_001161862.1
XM_011539808.2	3864	UTR 3			XP_011538110.1
XM_011539809.2	3864	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	3864	Missense Mutation	CCT,CTT	P1077L	NP_001165401.1
NM_001171931.1	3864	Intron			NP_001165402.1
NM_001171932.1	3864	Intron			NP_001165403.1
NM_001171933.1	3864	Intron			NP_001165404.1
NM_001171934.1	3864	Intron			NP_001165405.1
NM_001171935.1	3864	Intron			NP_001165406.1
NM_001171936.1	3864	Intron			NP_001165407.1
NM_022124.5	3864	Missense Mutation	CCT,CTT	P1077L	NP_071407.4
NM_052836.3	3864	Intron			NP_443068.1
XM_006717940.3	3864	Missense Mutation	CCT,CTT	P1142L	XP_006718003.1
XM_006717942.3	3864	Missense Mutation	CCT,CTT	P1120L	XP_006718005.1
XM_011540039.2	3864	Missense Mutation	CCT,CTT	P1142L	XP_011538341.1
XM_011540042.2	3864	Missense Mutation	CCT,CTT	P1142L	XP_011538344.1
XM_011540043.2	3864	Missense Mutation	CCT,CTT	P1142L	XP_011538345.1
XM_011540044.2	3864	Missense Mutation	CCT,CTT	P1097L	XP_011538346.1
XM_011540045.2	3864	Missense Mutation	CCT,CTT	P1142L	XP_011538347.1
XM_011540046.2	3864	Missense Mutation	CCT,CTT	P962L	XP_011538348.1
XM_011540047.2	3864	Missense Mutation	CCT,CTT	P748L	XP_011538349.1
XM_011540048.2	3864	Missense Mutation	CCT,CTT	P1142L	XP_011538350.1
XM_011540049.2	3864	Missense Mutation	CCT,CTT	P1142L	XP_011538351.1
XM_011540051.2	3864	Missense Mutation	CCT,CTT	P1142L	XP_011538353.1
XM_011540052.2	3864	Intron			XP_011538354.1
XM_017016499.1	3864	Missense Mutation	CCT,CTT	P1122L	XP_016871988.1
XM_017016500.1	3864	Missense Mutation	CCT,CTT	P1142L	XP_016871989.1
XM_017016501.1	3864	Missense Mutation	CCT,CTT	P288L	XP_016871990.1
XM_017016502.1	3864	Missense Mutation	CCT,CTT	P288L	XP_016871991.1
XM_017016503.1	3864	Intron			XP_016871992.1
XM_017016504.1	3864	Intron			XP_016871993.1
XM_017016505.1	3864	Intron			XP_016871994.1
XM_017016506.1	3864	Intron			XP_016871995.1
XM_017016507.1	3864	Intron			XP_016871996.1
XM_017016508.1	3864	Intron			XP_016871997.1

View Full Product Details