Variant #0000335639 (NC_000023.10:g.135292017T>C, NC_000023.10(NM_001159702.2):c.889-13T>C (FHL1))

Chromosome X
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.135292017T>C
DNA change (hg38) g.136209858T>C
Published as FHL1(NM_001159699.1):c.737-13T>C (p.(=)), FHL1(NM_001159702.2):c.889-13T>C, FHL1(NM_001159704.1):c.689-13T>C, FHL1(NM_001159704.1):c.689-13_689-8de...
ISCN -
DB-ID FHL1_000051 See all 6 reported entries
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +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     
FHL1 NM_001159702.2 -?/. - c.889-13T>C r.(=) p.(=)
MAP7D3 NM_024597.3 -?/. - c.*8668A>G r.(=) p.(=)


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