Variant #0000562512 (NC_000017.10:g.59485758C>T, NM_005994.3:c.2030C>T (TBX2))

Chromosome 17
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.59485758C>T
DNA change (hg38) g.61408397C>T
Published as TBX2(NM_005994.3):c.2030C>T (p.(Pro677Leu))
ISCN -
DB-ID C17orf82_000001
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0078 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-11-27 17:27:23 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TBX2 NM_005994.3 -?/. - c.2030C>T r.(?) p.(Pro677Leu)
C17orf82 NM_203425.1 -?/. - c.-3579C>T r.(?) p.(=)


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