Variant #0000703842 (NC_000010.10:g.43600496C>T, NM_020975.4:c.722C>T (RET))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.43600496C>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID RET_000293
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1178140696
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2020-11-09 14:53:02 +01:00 (CET)
Date last edited 2022-09-26 12:22:42 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RET NM_020975.4 -?/. - c.722C>T r.(?) p.(Ala241Val)


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