Variant #0000620476 (NC_000001.10:g.201346745C>A, NC_000001.10(NM_001001430.2):c.-15+6G>T (TNNT2))

Chromosome 1
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.201346745C>A
DNA change (hg38) g.201377617C>A
Published as TNNT2(NM_001276347.1):c.-148+6G>T
ISCN -
DB-ID LAD1_000003
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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TNNT2 NM_001001430.2 -?/. - c.-15+6G>T r.(=) p.(=)
LAD1 NM_005558.3 -?/. - c.*4271G>T r.(=) p.(=)


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