Product Details

SNP ID

rs62001038

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.7:108150081 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAACTAGGCTGTCGTCACTATCTTC[C/T]TTTTTCACAGTCCTGTCTGAAGGAG

Phenotype

MIM: 601581

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NRCAM PubMed Links

Gene Details

Gene

NRCAM

Gene Name

neuronal cell adhesion molecule

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037132.2	3903	Silent Mutation	AAA,AAG	K1248K	NP_001032209.1
NM_001193582.1	3903	Silent Mutation	AAA,AAG	K1155K	NP_001180511.1
NM_001193583.1	3903	Silent Mutation	AAA,AAG	K1136K	NP_001180512.1
NM_001193584.1	3903	Silent Mutation	AAA,AAG	K1124K	NP_001180513.1
NM_005010.4	3903	Silent Mutation	AAA,AAG	K1127K	NP_005001.3
XM_005250373.2	3903	Silent Mutation	AAA,AAG	K1248K	XP_005250430.1
XM_005250383.2	3903	Silent Mutation	AAA,AAG	K1158K	XP_005250440.1
XM_005250385.2	3903	Silent Mutation	AAA,AAG	K1143K	XP_005250442.1
XM_006716003.1	3903	Silent Mutation	AAA,AAG	K1252K	XP_006716066.1
XM_006716007.1	3903	Silent Mutation	AAA,AAG	K1240K	XP_006716070.1
XM_006716012.1	3903	Silent Mutation	AAA,AAG	K1159K	XP_006716075.1
XM_006716014.1	3903	Silent Mutation	AAA,AAG	K1147K	XP_006716077.1
XM_011516253.1	3903	Silent Mutation	AAA,AAG	K1255K	XP_011514555.1
XM_011516255.1	3903	Silent Mutation	AAA,AAG	K1255K	XP_011514557.1
XM_011516256.1	3903	Silent Mutation	AAA,AAG	K1251K	XP_011514558.1
XM_011516257.1	3903	Silent Mutation	AAA,AAG	K1249K	XP_011514559.1
XM_011516258.1	3903	Silent Mutation	AAA,AAG	K1249K	XP_011514560.1
XM_011516259.1	3903	Silent Mutation	AAA,AAG	K1245K	XP_011514561.1
XM_011516261.1	3903	Silent Mutation	AAA,AAG	K1239K	XP_011514563.1
XM_011516262.1	3903	Silent Mutation	AAA,AAG	K1236K	XP_011514564.1
XM_011516265.2	3903	Intron			XP_011514567.1
XM_011516266.2	3903	Intron			XP_011514568.1
XM_011516267.1	3903	Silent Mutation	AAA,AAG	K1162K	XP_011514569.1
XM_011516268.2	3903	Silent Mutation	AAA,AAG	K1159K	XP_011514570.1
XM_011516269.1	3903	Silent Mutation	AAA,AAG	K1150K	XP_011514571.1
XM_011516270.1	3903	Silent Mutation	AAA,AAG	K1146K	XP_011514572.1
XM_011516271.1	3903	Silent Mutation	AAA,AAG	K1130K	XP_011514573.1
XM_017012236.1	3903	Silent Mutation	AAA,AAG	K1242K	XP_016867725.1
XM_017012237.1	3903	Silent Mutation	AAA,AAG	K1236K	XP_016867726.1
XM_017012238.1	3903	Silent Mutation	AAA,AAG	K1232K	XP_016867727.1
XM_017012239.1	3903	Silent Mutation	AAA,AAG	K1230K	XP_016867728.1
XM_017012240.1	3903	Silent Mutation	AAA,AAG	K1229K	XP_016867729.1
XM_017012241.1	3903	Silent Mutation	AAA,AAG	K1233K	XP_016867730.1
XM_017012242.1	3903	Silent Mutation	AAA,AAG	K1217K	XP_016867731.1
XM_017012243.1	3903	Silent Mutation	AAA,AAG	K1201K	XP_016867732.1
XM_017012244.1	3903	Silent Mutation	AAA,AAG	K1200K	XP_016867733.1
XM_017012245.1	3903	Silent Mutation	AAA,AAG	K1197K	XP_016867734.1
XM_017012246.1	3903	Silent Mutation	AAA,AAG	K1149K	XP_016867735.1
XM_017012247.1	3903	Silent Mutation	AAA,AAG	K1140K	XP_016867736.1
XM_017012248.1	3903	Silent Mutation	AAA,AAG	K1140K	XP_016867737.1
XM_017012249.1	3903	Silent Mutation	AAA,AAG	K1139K	XP_016867738.1
XM_017012250.1	3903	Silent Mutation	AAA,AAG	K1143K	XP_016867739.1
XM_017012251.1	3903	Silent Mutation	AAA,AAG	K1137K	XP_016867740.1
XM_017012252.1	3903	Silent Mutation	AAA,AAG	K1136K	XP_016867741.1
XM_017012253.1	3903	Silent Mutation	AAA,AAG	K1141K	XP_016867742.1
XM_017012254.1	3903	Silent Mutation	AAA,AAG	K1133K	XP_016867743.1
XM_017012255.1	3903	Silent Mutation	AAA,AAG	K1133K	XP_016867744.1
XM_017012256.1	3903	Silent Mutation	AAA,AAG	K1137K	XP_016867745.1
XM_017012257.1	3903	Silent Mutation	AAA,AAG	K1136K	XP_016867746.1
XM_017012258.1	3903	UTR 3			XP_016867747.1
XM_017012259.1	3903	UTR 3			XP_016867748.1

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