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chr7:6026766 C>T

Annotations

GenePMS2
TranscriptNM_000535.6
cDNAc.1630G>A
Proteinp.D544N
Functionmissense
Localizationexon
hg19chr7:6026766 C>T

Synonyms

TranscriptcDNAProtein
NM_001322008.1c.1312G>Ap.D438N
NM_001322010.1c.1069G>Ap.D357N
NM_001322004.1c.1225G>Ap.D409N
NM_001322006.1c.1474G>Ap.D492N
NM_001322007.1c.1312G>Ap.D438N
NM_001322013.1c.1057G>Ap.D353N
NM_001322003.1c.1225G>Ap.D409N
NM_001322005.1c.1225G>Ap.D409N
NM_001322009.1c.1225G>Ap.D409N
NM_001322011.1c.697G>Ap.D233N
NM_001322012.1c.697G>Ap.D233N
NM_001322014.1c.1630G>Ap.D544N
NM_001322015.1c.1321G>Ap.D441N
NR_136154.1n.1717G>A

Frequency in gnomAD

GenomeExome
MAX
AFR
AMR
ASJ
EAS
FIN
NFE
SAS

ClinVar

IDPhenotypeEffect
RCV000477471.3Lynch syndromeVUS
RCV000627724.1Hereditary nonpolyposis colon cancerVUS
RCV000222810.2Hereditary cancer-predisposing syndromeVUS