Product Details

SNP ID
rs535226662
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:51616880 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTGGCAGCTAACTCTTTGTGAAGGG[C/T]GAAATAGAATGAAGAGTCATGACTG
Phenotype
MIM: 606702
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LOC101927082 PubMed Links

Gene Details

Gene
LOC101927082
Gene Name
uncharacterized LOC101927082
There are no transcripts associated with this gene.

Gene
PKHD1
Gene Name
polycystic kidney and hepatic disease 1 (autosomal recessive)
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_138694.3 13812 UTR 3 NP_619639.3
NM_170724.2 13812 Intron NP_733842.2
XM_011514680.2 13812 UTR 3 XP_011512982.1
XM_011514682.2 13812 UTR 3 XP_011512984.1
XM_011514683.2 13812 UTR 3 XP_011512985.1
XM_011514684.2 13812 UTR 3 XP_011512986.1
XM_011514685.1 13812 Intron XP_011512987.1
XM_011514686.2 13812 Intron XP_011512988.1
XM_011514687.1 13812 Intron XP_011512989.1
XM_011514688.2 13812 Intron XP_011512990.1
XM_011514690.2 13812 UTR 3 XP_011512992.1
XM_011514691.2 13812 UTR 3 XP_011512993.1
XM_017010944.1 13812 UTR 3 XP_016866433.1
XM_017010945.1 13812 UTR 3 XP_016866434.1
XM_017010946.1 13812 UTR 3 XP_016866435.1
XM_017010947.1 13812 UTR 3 XP_016866436.1
XM_017010948.1 13812 UTR 3 XP_016866437.1
XM_017010949.1 13812 UTR 3 XP_016866438.1
XM_017010950.1 13812 Intron XP_016866439.1
XM_017010951.1 13812 Intron XP_016866440.1
XM_017010952.1 13812 Intron XP_016866441.1

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