rs21

Variant names:

• chr7-11557307-G-A
• rs21
• NM_015204.3:c.1454-14190C>T

Your query was ambiguous. Multiple possible variants found:

• chr7-11557307-G-A
• chr7-11557307-G-C

Variant summary

Our verdict is Benign. The variant received -12 ACMG points: 0P and 12B. BP4_Strong BA1

The NM_015204.3(THSD7A):​c.1454-14190C>T variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant allele was found at a frequency of 0.596 in 151,782 control chromosomes in the GnomAD database, including 27,430 homozygotes. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: 𝑓 0.60 (27430 hom., cov: 32)
• Consequence: THSD7A NM_015204.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -0.117
• Publications: 0 publications found

Genes affected

THSD7A (HGNC:22207): (thrombospondin type 1 domain containing 7A) The protein encoded by this gene is found almost exclusively in endothelial cells from placenta and umbilical cord. The encoded protein appears to interact with alpha(V)beta(3) integrin and paxillin to inhibit endothelial cell migration and tube formation. This protein may be involved in cytoskeletal organization. Variations in this gene may be associated with low bone mineral density in osteoporosis. [provided by RefSeq, Aug 2010]

ACMG classification

Our verdict: Benign. The variant received -12 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-1.01).
• BA1: GnomAd4 highest subpopulation (AFR) allele frequency at 95% confidence interval = 0.705 is higher than 0.05.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
THSD7A	NM_015204.3	c.1454-14190C>T		intron_variant	Intron 4 of 27	ENST00000423059.9	NP_056019.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
THSD7A	ENST00000423059.9	c.1454-14190C>T		intron_variant	Intron 4 of 27	5	NM_015204.3	ENSP00000406482.2

Frequencies

GnomAD3 genomes AF: 0.595 AC: 90312 AN: 151662 Hom.: 27396 Cov.: 32

Gnomad AFR AF: 0.711

Gnomad AMI AF: 0.353

Gnomad AMR AF: 0.651

Gnomad ASJ AF: 0.593

Gnomad EAS AF: 0.557

Gnomad SAS AF: 0.531

Gnomad FIN AF: 0.508

Gnomad MID AF: 0.680

Gnomad NFE AF: 0.536

Gnomad OTH AF: 0.603

We have no GnomAD4 exomes data on this position. Probably position not covered by the project.

GnomAD4 genome AF: 0.596 AC: 90399 AN: 151782 Hom.: 27430 Cov.: 32 AF XY: 0.593 AC XY: 44008 AN XY: 74166

African (AFR) AF: 0.711 AC: 29472 AN: 41424

American (AMR) AF: 0.651 AC: 9915 AN: 15232

Ashkenazi Jewish (ASJ) AF: 0.593 AC: 2055 AN: 3468

East Asian (EAS) AF: 0.557 AC: 2875 AN: 5162

South Asian (SAS) AF: 0.531 AC: 2554 AN: 4812

European-Finnish (FIN) AF: 0.508 AC: 5343 AN: 10522

Middle Eastern (MID) AF: 0.673 AC: 198 AN: 294

European-Non Finnish (NFE) AF: 0.536 AC: 36400 AN: 67858

Other (OTH) AF: 0.603 AC: 1266 AN: 2100

Alfa AF: 0.576 Hom.: 10001

Bravo AF: 0.612

Asia WGS AF: 0.532 AC: 1845 AN: 3472

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-1.0
CADD	Benign	2.3
DANN	Benign	0.33
PhyloP100		-0.12
Mutation Taster		=100/0	polymorphism (auto)

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Other links and lift over

dbSNP: rs21; hg19: chr7-11596934;